Calf Garments RCG10
Contents
1. Restep DVT System Warranty Reprocessed Products Stryker warrants all reprocessed products subject to the exceptions provided herein to be free from defects in reprocessing and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for one use in accordance with the instructions for use of such product STRYKER SHALL NOT BE LIABLE FOR ANY DAMAGES TO THE EXTENT CAUSED BY ANY DEFECT IN MATERIAL WORKMANSHIP OR DESIGN BY THE ORIGINAL MANUFACTURER OF THE PRODUCT OR ANY ACT OR OMISSION OF THE ORIGINAL MANUFACTURER OF THE PRODUCT Products for which Stryker is the Original Manufacturer Stryker warrants all products for which it is the original manufacturer subject to the exceptions provided herein to be free from defects in design materials and workmanship and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for a period of one year from the date of purchase General Warranty Terms Applicable to All Products TO THE FULLEST EXTENT PERMITTED BY LAW THE EXPRESS WARRANTY SET FORTH HEREIN IS THE ONLY WARRANTY APPLICABLE TO THE PRODUCTS AND IS EXPRESSLY IN LIEU OF ANY OTHER WARRANTY BY STRYKER EXPRESSED OR IMPLIED INCLUDING BUT NOT LIMITED TO ANY IMPLIED WARRANTY OR MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE IN NO EVENT WILL STRYKER S LIABILITY ARISING IN CONNECTION WITH THE SALE OF THE PR2. Stryker will in its sole discretion 1 replace the product at no charge with a product that is at least functionally equivalent to the original product or 2 refund the purchase price of the product If a refund is provided by Stryker the product for which the refund is provided must be returned to Stryker and will become Stryker s property In any event Stryker s liability for breach of warranty shall be limited to the replacement value of the defective or non conforming part or component lf Stryker determines in its reasonable discretion that the claimed defect or non conformance in the product is excluded from warranty coverage as described hereunder it will notify the customer of such determination and will provide an estimate of the cost of repair of the product In such an event any repair would be performed at Stryker s standard rates Products and product components repaired or replaced under this warranty continue to be warranted as described herein during the initial applicable warranty period or if the initial warranty period has expired by the time the product is repaired or replaced for thirty 30 days after delivery of the repaired or replaced product When a product or component is replaced the item provided in replacement will be the customer s property and the replaced item will be Stryker s property If a refund is provided by Stryker the product for which the refund is provided must be returned to Stryker and will be
3. end of the cord into the top of the pump The BATTERY CHARGE light will flash green while the unit is charging The unit may be used while it is being charged When fully charged after 16 48 hours an audible double beep is presented once and the BATTERY CHARGE light green will be lit constantly Ensure the TYPE light indicates LEG GARMENT If not press the TYPE button until this light is illuminated Ensure the MODE light is not lit for SINGLE GARMENT If only one garment is needed press the MODE button to select SINGLE GARMENT and store the unused garment and tube for later use The pump is now ready for use Refer to the user operating manual for complete information on the use of the system Indications Intermittent Pneumatic Compression IPC is indicated for use for the prevention of deep vein thrombosis due to the presence of risk factors for thrombus formation during orthopedic trauma urologic neurology critical care general medicine obstetrics and general surgery stryker Sustainability Solutions Non Sterile Manufactured For Stryker Sustainability Solutions 1810 W Drake Dr DO NOT Reuse Consult Instruction Tempe AZ USA 85283 for Use Pack contains one Pair Compression Sleeves S Manufacture Thigh Garments RT G30 Universal size up to 26 0 66m thigh circumference Caution Federal U S A law restricts this device to sale by or on the order of a physician Recommend
4. provided by Stryker the product for which the refund is provided must be returned to Stryker and will become Stryker s property In any event Stryker s liability for breach of warranty shall be limited to the replacement value of the defective or non conforming part or component lf Stryker determines in its reasonable discretion that the claimed defect or non conformance in the product is excluded from warranty coverage as described hereunder it will notify the customer of such determination and will provide an estimate of the cost of repair of the product In such an event any repair would be performed at Stryker s standard rates Products and product components repaired or replaced under this warranty continue to be warranted as described herein during the initial applicable warranty period or if the initial warranty period has expired by the time the product is repaired or replaced for thirty 30 days after delivery of the repaired or replaced product When a product or component is replaced the item provided in replacement will be the customer s property and the replaced item will be Stryker s property If a refund is provided by Stryker the product for which the refund is provided must be returned to Stryker and will become Stryker s property
5. thirty 30 days of the expiration of the applicable warranty period Stryker will in its sole discretion 1 replace the product at no charge with a product that is at least functionally equivalent to the original product or 2 refund the purchase price of the product If a refund is provided by Stryker the product for which the refund is provided must be returned to Stryker and will become Stryker s property In any event Stryker s liability for breach of warranty shall be limited to the replacement value of the defective or non conforming part or component lf Stryker determines in its reasonable discretion that the claimed defect or non conformance in the product is excluded from warranty coverage as described hereunder it will notify the customer of such determination and will provide an estimate of the cost of repair of the product In such an event any repair would be performed at Stryker s standard rates Products and product components repaired or replaced under this warranty continue to be warranted as described herein during the initial applicable warranty period or if the initial warranty period has expired by the time the product is repaired or replaced for thirty 30 days after delivery of the repaired or replaced product When a product or component is replaced the item provided in replacement will be the customer s property and the replaced item will be Stryker s property If a refund is provided by Stryker the product for
6. CULAR PURPOSE IN NO EVENT WILL STRYKER S LIABILITY ARISING IN CONNECTION WITH THE SALE OF THE PRODUCT WHETHER UNDER THE THEORIES OF BREACH OF CONTRACT TORT MISREPRESENTATION FRAUD WARRANTY NEGLIGENCE STRICT LIABILITY OR ANY OTHER THEORY OF LAW EXCEED THE PURCHASE PRICE CURRENT MARKET VALUE OR RESIDUAL VALUE OF THE PRODUCTS WHICHEVER IS LESS STRYKER SHALL NOT BE LIABLE FOR INDIRECT SPECIAL INCIDENTAL PUNITIVE OR CONSEQUENTIAL DAMAGES RESULTING FROM ANY BREACH OF WARRANTY OR UNDER ANY OTHER LEGAL THEORY This warranty shall apply only to the original end user purchaser of products directly from Stryker or a Stryker authorized distributor This warranty may not be transferred or assigned without the express written consent of Stryker This warranty does not apply to 1 products that have been misused neglected modified altered adjusted tampered with improperly installed or refurbished 2 products that have been repaired by any person other than Stryker personnel without the prior written consent of Stryker 3 products that have been subjected to unusual stress or have not been maintained in accordance with the instructions in the user manual or as demonstrated by a Stryker representative 4 products on which any original serial numbers or other identification marks have been removed or destroyed or 5 products that have been repaired with any unauthorized or non Stryker components If a valid warranty claim is received within
7. NECTION WITH THE SALE OF THE PRODUCT WHETHER UNDER THE THEORIES OF BREACH OF CONTRACT TORT MISREPRESENTATION FRAUD WARRANTY NEGLIGENCE STRICT LIABILITY OR ANY OTHER THEORY OF LAW EXCEED THE PURCHASE PRICE CURRENT MARKET VALUE OR RESIDUAL VALUE OF THE PRODUCTS WHICHEVER IS LESS STRYKER SHALL NOT BE LIABLE FOR INDIRECT SPECIAL INCIDENTAL PUNITIVE OR CONSEQUENTIAL DAMAGES RESULTING FROM ANY BREACH OF WARRANTY OR UNDER ANY OTHER LEGAL THEORY This warranty shall apply only to the original end user purchaser of products directly from Stryker or a Stryker authorized distributor This warranty may not be transferred or assigned without the express written consent of Stryker This warranty does not apply to 1 products that have been misused neglected modified altered adjusted tampered with improperly installed or refurbished 2 products that have been repaired by any person other than Stryker personnel without the prior written consent of Stryker 3 products that have been subjected to unusual stress or have not been maintained in accordance with the instructions in the user manual or as demonstrated by a Stryker representative 4 products on which any original serial numbers or other identification marks have been removed or destroyed or 5 products that have been repaired with any unauthorized or non Stryker components If a valid warranty claim is received within thirty 30 days of the expiration of the applicable warranty period
8. ODUCT WHETHER UNDER THE THEORIES OF BREACH OF CONTRACT TORT MISREPRESENTATION FRAUD WARRANTY NEGLIGENCE STRICT LIABILITY OR ANY OTHER THEORY OF LAW EXCEED THE PURCHASE PRICE CURRENT MARKET VALUE OR RESIDUAL VALUE OF THE PRODUCTS WHICHEVER IS LESS STRYKER SHALL NOT BE LIABLE FOR INDIRECT SPECIAL INCIDENTAL PUNITIVE OR CONSEQUENTIAL DAMAGES RESULTING FROM ANY BREACH OF WARRANTY OR UNDER ANY OTHER LEGAL THEORY This warranty shall apply only to the original end user purchaser of products directly from Stryker or a Stryker authorized distributor This warranty may not be transferred or assigned without the express written consent of Stryker This warranty does not apply to 1 products that have been misused neglected modified altered adjusted tampered with improperly installed or refurbished 2 products that have been repaired by any person other than Stryker personnel without the prior written consent of Stryker 3 products that have been subjected to unusual stress or have not been maintained in accordance with the instructions in the user manual or as demonstrated by a Stryker representative 4 products on which any original serial numbers or other identification marks have been removed or destroyed or 5 products that have been repaired with any unauthorized or non Stryker components If a valid warranty claim is received within thirty 30 days of the expiration of the applicable warranty period Stryker will in its sole di
9. Patients should be instructed in the proper use of the system and should report any problems to the nursing staff The system should be used continuously until the person is fully ambulatory The therapy can continue with calf garments for patients with limited mobility If the garment cannot be applied to a limb during surgery it may be applied to the limb once the patient reaches the recovery room For a non surgical patient the system should be applied as soon as the risk of DVT is identified Contraindications tie Restep system should not be used in the following conditions Severe arteriosclerosis or active infection e Suspected or known acute DVT e Severe congestive heart failure or any condition where increased fluid to the heart may be detrimental e Existing pulmonary edema e Local skin or tissue conditions in which the garments would interfere If in doubt refer to the patient s physician before using device Cautions Garments should be removed immediately if the patient experiences any unexplained sensations numbness or pain When used for DVT prophylaxis continuous use is recommended and any prolonged interruption of therapy should be done in consultation with the patient s physician Garments are single patient use non sterile and latex free Garment bladders are PVC free For use with Restep Pump RSP101 only Made in the Dominican Republic RCS Rev D 09 2012 RM705001 Restep is a registered t
10. Republic RCS Rev D 09 2012 RM705003 Restep is a registered trademark of Stryker Corporation Restep DVT System Warranty Reprocessed Products Stryker warrants all reprocessed products subject to the exceptions provided herein to be free from defects in reprocessing and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for one use in accordance with the instructions for use of such product STRYKER SHALL NOT BE LIABLE FOR ANY DAMAGES TO THE EXTENT CAUSED BY ANY DEFECT IN MATERIAL WORKMANSHIP OR DESIGN BY THE ORIGINAL MANUFACTURER OF THE PRODUCT OR ANY ACT OR OMISSION OF THE ORIGINAL MANUFACTURER OF THE PRODUCT Products for which Stryker is the Original Manufacturer Stryker warrants all products for which it is the original manufacturer subject to the exceptions provided herein to be free from defects in design materials and workmanship and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for a period of one year from the date of purchase General Warranty Terms Applicable to All Products TO THE FULLEST EXTENT PERMITTED BY LAW THE EXPRESS WARRANTY SET FORTH HEREIN IS THE ONLY WARRANTY APPLICABLE TO THE PRODUCTS AND IS EXPRESSLY IN LIEU OF ANY OTHER WARRANTY BY STRYKER EXPRESSED OR IMPLIED INCLUDING BUT NOT LIMITED TO ANY IMPLIED WARRANTY OR MERCHANTABILITY OR FITNESS FOR A PARTI
11. T MARKET VALUE OR RESIDUAL VALUE OF THE PRODUCTS WHICHEVER IS LESS STRYKER SHALL NOT BE LIABLE FOR INDIRECT SPECIAL INCIDENTAL PUNITIVE OR CONSEQUENTIAL DAMAGES RESULTING FROM ANY BREACH OF WARRANTY OR UNDER ANY OTHER LEGAL THEORY This warranty shall apply only to the original end user purchaser of products directly from Stryker or a Stryker authorized distributor This warranty may not be transferred or assigned without the express written consent of Stryker This warranty does not apply to 1 products that have been misused neglected modified altered adjusted tampered with improperly installed or refurbished 2 products that have been repaired by any person other than Stryker personnel without the prior written consent of Stryker 3 products that have been subjected to unusual stress or have not been maintained in accordance with the instructions in the user manual or as demonstrated by a Stryker representative 4 products on which any original serial numbers or other identification marks have been removed or destroyed or 5 products that have been repaired with any unauthorized or non Stryker components If a valid warranty claim is received within thirty 30 days of the expiration of the applicable warranty period Stryker will in its sole discretion 1 replace the product at no charge with a product that is at least functionally equivalent to the original product or 2 refund the purchase price of the product If a refund is
12. ash green while the unit is charging The unit may be used while it is being charged When fully charged after 16 48 hours an audible double beep is presented once and the BATTERY CHARGE light green will be lit constantly Ensure the TYPE light indicates LEG GARMENT If not press the TYPE button until this light is illuminated Ensure the MODE light is not lit for SINGLE GARMENT If only one garment is needed press the MODE button to select SINGLE GARMENT and store the unused garment and tube for later use The pump is now ready for use Refer to the user operating manual for complete information on system use Indications Intermittent Pneumatic Compression IPC is indicated for use of the prevention of deep vein thrombosis due to the presence of risk factors for thrombus formation during orthopedic trauma urologic neurology critical care general medicine obstetrics and general surgery stryker Sustainability Solutions Non Sterile Manufactured For Stryker Sustainability Solutions 1810 W Drake Dr DO NOT Reuse Consult Instruction Tempe AZ USA 85283 for Use Pack contains one Pair Compression Sleeves S Manufacture Calf Garments RCG10 Universal size up to 20 0 51m circumference Caution Federal U S A law restricts this device to sale by or on the order of a physician Recommendations Garments should be removed regularly to inspect the skin Patients should be instruc
13. ations Garments should be removed regularly to inspect the skin Patients should be instructed in the proper use of the system and should report any problems to the nursing staff The system should be used continuously until the person is fully ambulatory The therapy can continue with leg garments for patients with limited mobility If the garment cannot be applied to a limb during surgery it may be applied to the limb once the patient reaches the recovery room For a non surgical patient the system should be applied as soon as the risk of DVT is identified Contraindications The Restep system should not be used in the following conditions e Severe arteriosclerosis or active infection e Suspected or known acute DVT e Severe congestive heart failure or any condition where increased fluid to the heart may be detrimental e Existing pulmonary edema e Local skin or tissue conditions in which the garments would interfere If in doubt refer to the patient s physician before using device Cautions Garments should be removed immediately if the patient experiences any unexplained sensations numbness or pain When used for DVT prophylaxis continuous use is recommended and any prolonged interruption of therapy should be done in consultation with the patient s physician Garments are single patient use non sterile and latex free Garment bladders are PVC free For use with Restep Pump RSP101 only Made in the Dominican
14. come Stryker s property esten DVT System Instructions for use Secure the pump at the foot of the bed or in place of use Attach the tube set to the pump connector by pushing in the silver latch on the female pump connector and then inserting the male tube connector into the pump connector until a click is heard Garments may be used on either leg Unfold the garment s and position the inflatable center bladder directly behind the patient s calf with the cut out BEHIND the knee The outlet tube on the garment should not be in direct contact with the patient s skin SNUGLY wrap the garment s around the patient s leg s and secure the hook tabs Attach the garment s to the tube set by pushing in the silver latch on the female tube connector and inserting the male garment connector firmly into the tube connector until a click is heard Ensure the pump is held firmly onto the bed frame while used in bed During ambulation or transpor tation ensure that the pump is secured Rotate the outlet tube on the garment to eliminate kinks in the tubing Tubing may become a trip hazard during ambulation if the shoulder strap is not used to secure excess tubing Turn the pump on by pressing the POWER button If the LOW BATTERY light is solid red and producing a constant audible alarm the battery will need to be charged To charge the unit plug the supplied power adaptor into a power outlet and then plug the round connector at the
15. esten DVT System Instructions for use Secure the pump at the foot of the bed or in place of use Attach the tube set to the pump by pushing in the silver latch on the female pump connector and then inserting the male tube connector into the pump connector until a click is heard Garments may be used on either leg Unfold the garment s and position the inflatable center bladder directly behind the patient s calf The outlet tube on the garment should not be in direct contact with the patient s skin SNUGLY wrap the garment s around the patient s leg s and secure the hook tabs Attach the garment s to the tube set by pushing in the silver latch on the female tube connector and inserting the male garment connector firmly into the tube connector until a click is heard Ensure the pump is held firmly onto the bed frame while used in bed During ambulation or transportation ensure that the pump is secured Rotate the outlet tube on the garment to eliminate kinks in the tubing Tubing may become a trip hazard during ambulation if the shoulder strap is not used to secure excess tubing Turn the pump on by pressing the POWER button If the LOW BATTERY light is solid red and producing a constant audible alarm the battery will need to be charged To charge the unit plug the supplied power adaptor into a power outlet and then plug the round connector at the end of the cord into the top of the pump The BATTERY CHARGE light will fl
16. hen fully charged after 16 48 hours an audible double beep is presented once and the BATTERY CHARGE light green will be lit constantly Ensure the TYPE light indicates FOOT GARMENT If not press the TYPE button until the light is illuminated Ensure the MODE light is not lit for SINGLE GARMENT If only one garment is needed press the MODE button to select SINGLE GARMENT The pump is now ready for use Refer to the user operating manual for complete information on the use of the system Indications Intermittent Pneumatic Compression IPC is indicated for use for the prevention of deep vein thrombosis due to the presence of risk factors for thrombus formation during orthopedic trauma urologic neurology critical care general medicine obstetrics and general surgery stryker Sustainability Solutions Non Sterile Manufactured For Stryker Sustainability Solutions 1810 W Drake Dr DO NOT Reuse Consult Instruction Tempe AZ USA 85283 for Use Pack contains one Single Compression Sleeve a Manufacture Foot Garment RFG210 Universal size Caution Federal U S A law restricts this device to sale by or on the order of a physician Recommendations Garments should be removed regularly to inspect the skin Patients should be instructed in the proper use of the system and report any problems to the nursing staff The system should be used continuously until the person is fully ambulat
17. ory Foot garments should be removed before ambulating If the garment cannot be applied to a limb during surgery it may be applied to the limb once the patient reaches the recovery room For a non surgical patient the system should be applied as soon as the risk of DVT is identified Contraindications ine Restep system should not be used in the following conditions Severe arteriosclerosis or active infection e Suspected or known acute DVT e Severe congestive heart failure or any condition where increased fluid to the heart may be detrimental e Existing pulmonary edema e Local skin or tissue conditions in which the garments would interfere If in doubt refer to the patient s physician before using device Cautions Garments should be removed immediately if the patient experiences any unexplained sensations numbness or pain When used for DVT prophylaxis continuous use is recommended and any prolonged interruption of therapy should be done in consultation with the patient s physician Garments are single patient use non sterile and latex free Garment bladders are PVC free For use with Restep Pump RSP101 only Made in the Dominican Republic RCS Rev C 04 2012 RM705002 Restep is a registered trademark of Stryker Corporation Restep DVT System Warranty Reprocessed Products Stryker warrants all reprocessed products subject to the exceptions provided herein to be free from defects in reprocessing and
18. rademark of Stryker Corporation Restep DVT System Warranty Reprocessed Products Stryker warrants all reprocessed products subject to the exceptions provided herein to be free from defects in reprocessing and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for one use in accordance with the instructions for use of such product STRYKER SHALL NOT BE LIABLE FOR ANY DAMAGES TO THE EXTENT CAUSED BY ANY DEFECT IN MATERIAL WORKMANSHIP OR DESIGN BY THE ORIGINAL MANUFACTURER OF THE PRODUCT OR ANY ACT OR OMISSION OF THE ORIGINAL MANUFACTURER OF THE PRODUCT Products for which Stryker is the Original Manufacturer Stryker warrants all products for which it is the original manufacturer subject to the exceptions provided herein to be free from defects in design materials and workmanship and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for a period of one year from the date of purchase General Warranty Terms Applicable to All Products TO THE FULLEST EXTENT PERMITTED BY LAW THE EXPRESS WARRANTY SET FORTH HEREIN IS THE ONLY WARRANTY APPLICABLE TO THE PRODUCTS AND IS EXPRESSLY IN LIEU OF ANY OTHER WARRANTY BY STRYKER EXPRESSED OR IMPLIED INCLUDING BUT NOT LIMITED TO ANY IMPLIED WARRANTY OR MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE IN NO EVENT WILL STRYKER S LIABILITY ARISING IN CON
19. scretion 1 replace the product at no charge with a product that is at least functionally equivalent to the original product or 2 refund the purchase price of the product If a refund is provided by Stryker the product for which the refund is provided must be returned to Stryker and will become Stryker s property In any event Stryker s liability for breach of warranty shall be limited to the replacement value of the defective or non conforming part or component lf Stryker determines in its reasonable discretion that the claimed defect or non conformance in the product is excluded from warranty coverage as described hereunder it will notify the customer of such determination and will provide an estimate of the cost of repair of the product In such an event any repair would be performed at Stryker s standard rates Products and product components repaired or replaced under this warranty continue to be warranted as described herein during the initial applicable warranty period or if the initial warranty period has expired by the time the product is repaired or replaced for thirty 30 days after delivery of the repaired or replaced product When a product or component is replaced the item provided in replacement will be the customer s property and the replaced item will be Stryker s property If a refund is provided by Stryker the product for which the refund is provided must be returned to Stryker and will become Stryker s property e
20. sh green while the unit is charging The unit may be used while it is being charged When fully charged after 16 48 hours an audible double beep is presented once and the BATTERY CHARGE light green will be lit constantly Ensure the TYPE light indicates LEG GARMENT If not press the TYPE button until this light is illuminated Ensure the MODE light is not lit for SINGLE GARMENT If only one garment is needed press the MODE button to select SINGLE GARMENT and store the unused garment and tube for later use The pump is now ready for use Refer to the user operating manual for complete information on the use of the system Indications Intermittent Pneumatic Compression IPC is indicated for use for the prevention of deep vein thrombosis due to the presence of risk factors for thrombus formation during orthopedic trauma urologic neurology critical care general medicine obstetrics and general surgery stryker Sustainability Solutions Non Sterile Manufactured For Stryker Sustainability Solutions 1810 W Drake Dr DO NOT Reuse Consult Instruction Tempe AZ USA 85283 for Use Pack contains one Pair Compression Sleeves S Manufacture Bariatric Calf Garment RBG60 Size 20 to 26 0 51 to 0 66m calf circumference Caution Federal U S A law restricts this device to sale by or on the order of a physician Recommendations Garments should be removed regularly to inspect the skin
21. sten DVT System Instructions for use Secure the pump at the foot of the bed or in place of use Attach the tube set to the pump by pushing in the silver latch on the female pump connector and then inserting the male tube connector into the pump connector until a click is heard Garments may be used on either leg Unfold the garment s and position the inflatable center bladder directly behind the patient s calf The outlet tube on the garment should not be in direct contact with the patient s skin SNUGLY wrap the garment s around the patient s leg s and secure the hook tabs Attach the garment s to the tube set by pushing in the silver latch on the female tube connector and inserting the male garment connector firmly into the tube connector until a click is heard Ensure the pump is held firmly onto the bed frame while used in bed During ambulation or transportation ensure that the pump is secured Rotate the outlet tube on the garment to eliminate kinks in the tubing Tubing may become a trip hazard during ambulation if the shoulder strap is not used to secure excess tubing Turn the pump on by pressing the POWER button If the LOW BATTERY light is solid red and producing a constant audible alarm the battery will need to be charged To charge the unit plug the supplied power adaptor into a power outlet and then plug the round connector at the end of the cord into the top of the pump The BATTERY CHARGE light will fla
22. ted in the proper use of the system and should report any problems to the nursing staff The system should be used continuously until the person is fully ambulatory The therapy can continue with calf garments for patients with limited mobility If the garment cannot be applied to a limb during surgery it may be applied to the limb once the patient reaches the recovery room For a non surgical patient the system should be applied as soon as the risk of DVT is identified Contraindications e Restep system should not be used in the following conditions Severe arteriosclerosis or active infection e Suspected or known acute DVT e Severe congestive heart failure or any condition where increased fluid to the heart may be detrimental e Existing pulmonary edema e Local skin or tissue conditions in which the garments would interfere If in doubt refer to the patient s physician before using device Cautions Garments should be removed immediately if the patient experiences any unexplained sensations numbness or pain When used for DVT prophylaxis continuous use is recommended Any prolonged interruption of therapy should be done in consultation with the patient s physician Garments are single patient use non sterile and latex free Garment bladders are PVC free For use with Restep Pump RSP101 only Made in the Dominican Republic RCS Rev D 09 2012 RM705000 Restep is a registered trademark of Stryker Corporation
23. to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for one use in accordance with the instructions for use of such product STRYKER SHALL NOT BE LIABLE FOR ANY DAMAGES TO THE EXTENT CAUSED BY ANY DEFECT IN MATERIAL WORKMANSHIP OR DESIGN BY THE ORIGINAL MANUFACTURER OF THE PRODUCT OR ANY ACT OR OMISSION OF THE ORIGINAL MANUFACTURER OF THE PRODUCT Products for which Stryker is the Original Manufacturer Stryker warrants all products for which it is the original manufacturer subject to the exceptions provided herein to be free from defects in design materials and workmanship and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for a period of one year from the date of purchase General Warranty Terms Applicable to All Products TO THE FULLEST EXTENT PERMITTED BY LAW THE EXPRESS WARRANTY SET FORTH HEREIN IS THE ONLY WARRANTY APPLICABLE TO THE PRODUCTS AND IS EXPRESSLY IN LIEU OF ANY OTHER WARRANTY BY STRYKER EXPRESSED OR IMPLIED INCLUDING BUT NOT LIMITED TO ANY IMPLIED WARRANTY OR MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE IN NO EVENT WILL STRYKER S LIABILITY ARISING IN CONNECTION WITH THE SALE OF THE PRODUCT WHETHER UNDER THE THEORIES OF BREACH OF CONTRACT TORT MISREPRESENTATION FRAUD WARRANTY NEGLIGENCE STRICT LIABILITY OR ANY OTHER THEORY OF LAW EXCEED THE PURCHASE PRICE CURREN
24. which the refund is provided must be returned to Stryker and will become Stryker s property esten DVT System Instructions for use Secure the pump at the foot of the bed or in place of use Attach the tube set to the pump by pushing in the silver latch on the fe male pump connector and then inserting the male tube connec tor into the pump connector until a click is heard Garments may be used on either foot Unfold the garment s and position the inflatable center bladder directly below the arch of the patient s foot SNUGLY wrap the garment s around the pa tient s foot and secure the hook tabs Wrap the ankle straps around the back of the ankle and on top the foot Attach the garment s to the tube set by pushing in the silver latch on the female tube connector and inserting the male garment connector firmly into the tube connector until a click is heard Ensure the pump is held firmly onto the bed frame Foot garments should be removed prior to patient ambulation or transportation Turn the pump on by pressing the POWER but ton If the LOW BATTERY light is solid red and producing a constant audible alarm the battery will need to be charged To charge the unit plug the supplied power adaptor into a power outlet and then plug the round connector at the end of the cord into the top of the pump The BATTERY CHARGE light will flash green while the unit is charging The unit may be used while it is being charged W
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