An effective closed suction drain system requires maintenance of the system to preserve patency. The drain must not be allowed to occlude nor the reservoir to completely fill; and reservoir suction must be maintained in order for the system to function properly. Verify that the system is functioning properly. If the system is not maintained properly, surgical complications, including hematomas, may result.
In the event of occlusion of the drain, all wound drainage via the drain ceases. Careful attention to the drain will minimize the possibility of this problem. If occlusion does occur, the drain can be aspirated by connecting suction to the reservoir outlet or temporarily disconnecting the drain from the reservoir and applying suction directly to the drain.
If an air-tight seal between the drain and the skin where the drain emerges is not achieved, the air leak must be rectified, or the system must be converted to open drainage.
An airtight seal between all system components (drain, adaptor and reservoir) is necessary for proper system function.
Leaving the soft silicone elastomer drain implanted for any period of time so as to cause tissue in growth around the drain can interfere with easy removal and may affect the performance of the drain. The surgeon should monitor the patient’s rate of wound healing
Drain perforations or channels must lie within the wound or cavity to be drained, otherwise inadequate drainage may result.
To avoid the possibility of drain damage or breakage:
Avoid suturing through drains.
Drains should lie flat and in line with the skin exit areas.
Particular care should be taken to avoid any obstacles to the drain exit path.
Drains should be checked for free motion during closure to minimize the possibility of breakage.
Drain removal should be done gently by hand. Drains should not be handled with pointed, toothed or sharp instruments which could cause cuts or nicks and lead to subsequent structural failure of the drain.
Surgical removal may be necessary if drain is difficult to remove or breaks.
Do not bypass/inactivate anti-reflux valve.
Blood collected using the Evacuator should not be re-infused.
DO NOT use in patients who are allergic to materials used in BD™ Drain Products.
This is a single use device. DO NOT reuse.
DO NOT re-sterilize.
Trocar and evacuator are MR unsafe.
After use, this product may be a potential biohazard. Handle and dispose of in accordance with accepted medical practice and applicable local, state, and federal laws and regulations.
Precautions
Ensure that the wound site is dry and free of debris before closure.
The surgeon must determine the number of drains needed for an effective drainage of the entire wound site.
If the drain is occluded, irrigation and/or aspiration of the drain may be required.
The quality and quantity of drained fluid must be regularly monitored and reported to the surgeon.
Reservoir, once full, must be emptied per hospital protocols. Failure to do so will result in incomplete drainage.
Suction must be discontinued prior to the removal of the drain.
Before starting the Drainage Procedure, ensure that all the connections are tight and free of any obstructions within the drainage pathway.
Di(2-ethylhexyl) phthalate (DEHP) is a plasticizer used in some polyvinyl chloride medical devices. DEHP has been shown to produce a range of adverse effects in experimental animals, notably liver toxicity and testicular atrophy. Although the toxic and carcinogenic effects of DEHP have been well established in experimental animals, the ability of this compound to produce adverse effects in humans is controversial. There is no evidence that neonates, infants, pregnant and breast-feeding women exposed to DEHP experience any related adverse effects. However, a lack of evidence of causation between DEHP-PVC and any disease or adverse effect does not mean that there are no risks.
Contraindications
Closed Wound Suction System: Do not use for chest drainage.
Caution: Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.
Please consult product labels, inserts and instructions for use for any indications, contraindications, hazards, warnings, cautions and directions for use.
An effective closed suction drain system requires maintenance of the system to preserve patency. The drain must not be allowed to occlude nor the reservoir to completely fill; and reservoir suction must be maintained in order for the system to function properly. Verify that the system is functioning properly. If the system is not maintained properly, surgical complications, including hematomas, may result.
In the event of occlusion of the drain, all wound drainage via the drain ceases. Careful attention to the drain will minimize the possibility of this problem. If occlusion does occur, the drain can be aspirated by connecting suction to the reservoir outlet or temporarily disconnecting the drain from the reservoir and applying suction directly to the drain.
If an air-tight seal between the drain and the skin where the drain emerges is not achieved, the air leak must be rectified, or the system must be converted to open drainage.
An airtight seal between all system components (drain, adaptor and reservoir) is necessary for proper system function.
Leaving the soft silicone elastomer drain implanted for any period of time so as to cause tissue in growth around the drain can interfere with easy removal and may affect the performance of the drain. The surgeon should monitor the patient’s rate of wound healing
Drain perforations or channels must lie within the wound or cavity to be drained, otherwise inadequate drainage may result.
To avoid the possibility of drain damage or breakage:
Avoid suturing through drains.
Drains should lie flat and in line with the skin exit areas.
Particular care should be taken to avoid any obstacles to the drain exit path.
Drains should be checked for free motion during closure to minimize the possibility of breakage.
Drain removal should be done gently by hand. Drains should not be handled with pointed, toothed or sharp instruments which could cause cuts or nicks and lead to subsequent structural failure of the drain.
Surgical removal may be necessary if drain is difficult to remove or breaks.
Do not bypass/inactivate anti-reflux valve.
Blood collected using the Evacuator should not be re-infused.
DO NOT use in patients who are allergic to materials used in BD™ Drain Products.
This is a single use device. DO NOT reuse.
DO NOT re-sterilize.
Trocar and evacuator are MR unsafe.
After use, this product may be a potential biohazard. Handle and dispose of in accordance with accepted medical practice and applicable local, state, and federal laws and regulations.
Precautions
Ensure that the wound site is dry and free of debris before closure.
The surgeon must determine the number of drains needed for an effective drainage of the entire wound site.
If the drain is occluded, irrigation and/or aspiration of the drain may be required.
The quality and quantity of drained fluid must be regularly monitored and reported to the surgeon.
Reservoir, once full, must be emptied per hospital protocols. Failure to do so will result in incomplete drainage.
Suction must be discontinued prior to the removal of the drain.
Before starting the Drainage Procedure, ensure that all the connections are tight and free of any obstructions within the drainage pathway.
Di(2-ethylhexyl) phthalate (DEHP) is a plasticizer used in some polyvinyl chloride medical devices. DEHP has been shown to produce a range of adverse effects in experimental animals, notably liver toxicity and testicular atrophy. Although the toxic and carcinogenic effects of DEHP have been well established in experimental animals, the ability of this compound to produce adverse effects in humans is controversial. There is no evidence that neonates, infants, pregnant and breast-feeding women exposed to DEHP experience any related adverse effects. However, a lack of evidence of causation between DEHP-PVC and any disease or adverse effect does not mean that there are no risks.
Contraindications
Closed Wound Suction System: Do not use for chest drainage.
Caution: Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.
Please consult product labels, inserts and instructions for use for any indications, contraindications, hazards, warnings, cautions and directions for use.
An effective closed suction drain system requires maintenance of the system to preserve patency. The drain must not be allowed to occlude nor the reservoir to completely fill; and reservoir suction must be maintained in order for the system to function properly. Verify that the system is functioning properly. If the system is not maintained properly, surgical complications, including hematomas, may result.
In the event of occlusion of the drain, all wound drainage via the drain ceases. Careful attention to the drain will minimize the possibility of this problem. If occlusion does occur, the drain can be aspirated by connecting suction to the reservoir outlet or temporarily disconnecting the drain from the reservoir and applying suction directly to the drain.
If an air-tight seal between the drain and the skin where the drain emerges is not achieved, the air leak must be rectified, or the system must be converted to open drainage.
An airtight seal between all system components (drain, adaptor and reservoir) is necessary for proper system function.
Leaving the soft silicone elastomer drain implanted for any period of time so as to cause tissue in growth around the drain can interfere with easy removal and may affect the performance of the drain. The surgeon should monitor the patient’s rate of wound healing
Drain perforations or channels must lie within the wound or cavity to be drained, otherwise inadequate drainage may result.
To avoid the possibility of drain damage or breakage:
Avoid suturing through drains.
Drains should lie flat and in line with the skin exit areas.
Particular care should be taken to avoid any obstacles to the drain exit path.
Drains should be checked for free motion during closure to minimize the possibility of breakage.
Drain removal should be done gently by hand. Drains should not be handled with pointed, toothed or sharp instruments which could cause cuts or nicks and lead to subsequent structural failure of the drain.
Surgical removal may be necessary if drain is difficult to remove or breaks.
Do not bypass/inactivate anti-reflux valve.
Blood collected using the Evacuator should not be re-infused.
DO NOT use in patients who are allergic to materials used in BD™ Drain Products.
This is a single use device. DO NOT reuse.
DO NOT re-sterilize.
Trocar and evacuator are MR unsafe.
After use, this product may be a potential biohazard. Handle and dispose of in accordance with accepted medical practice and applicable local, state, and federal laws and regulations.
Precautions
Ensure that the wound site is dry and free of debris before closure.
The surgeon must determine the number of drains needed for an effective drainage of the entire wound site.
If the drain is occluded, irrigation and/or aspiration of the drain may be required.
The quality and quantity of drained fluid must be regularly monitored and reported to the surgeon.
Reservoir, once full, must be emptied per hospital protocols. Failure to do so will result in incomplete drainage.
Suction must be discontinued prior to the removal of the drain.
Before starting the Drainage Procedure, ensure that all the connections are tight and free of any obstructions within the drainage pathway.
Di(2-ethylhexyl) phthalate (DEHP) is a plasticizer used in some polyvinyl chloride medical devices. DEHP has been shown to produce a range of adverse effects in experimental animals, notably liver toxicity and testicular atrophy. Although the toxic and carcinogenic effects of DEHP have been well established in experimental animals, the ability of this compound to produce adverse effects in humans is controversial. There is no evidence that neonates, infants, pregnant and breast-feeding women exposed to DEHP experience any related adverse effects. However, a lack of evidence of causation between DEHP-PVC and any disease or adverse effect does not mean that there are no risks.
Contraindications
Closed Wound Suction System: Do not use for chest drainage.
Caution: Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.
Please consult product labels, inserts and instructions for use for any indications, contraindications, hazards, warnings, cautions and directions for use.
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Wound Drains | Channel Drains | BD/content/dam/bd-assets/bd-com/en-us/images/product-family/advanced-patient-monitoring/foresight-tissue-oximetry-sensor/foresight_iq-thumb.jpgBDClosed wound drains/content/dam/bd-assets/bd-com/en-us/logos/bd/header-bd-logo.svg072328Silicone Channel Drain (28 Fr)Round-Hubless, full fluted drain072292Silicone Channel Drain (32 Fr)Round-Hubless, full fluted drain072290Silicone Channel Drain (28F)Silicone Channel Drain, 28F, Round, Full Fluted, Hubless072235Silicone Channel Drain (24F) with Depth MarkingsSilicone Channel Drain, 24F, Round, Full Fluted, Hubless, Depth Markings072234Silicone Channel Drain (24 Fr)Round-Hubless, full fluted drain072231Silicone Channel Drain (19 Fr) with TrocarRound-Hubless, full fluted drain072230Silicone Channel Drain (19 Fr)Round-Hubless, full fluted drain072229Silicone Channel Drain (15F) with 4.7mm (3/16") TrocarSilicone Channel Drain, 15F, Round, Full Fluted, Hubless and packaged with 4.7mm (3/16") Trocar072228Silicone Channel Drain (15 Fr)Round-Hubless, full fluted drain072227Silicone Channel Drain (10F) with 3.2mm (1/8") TrocarSilicone Channel Drain, 10F, Round, Full Fluted, Hubless and packaged with 3.2mm (1/8") Trocar072226Silicone Channel Drain (10F)Silicone Channel Drain, 10F, Round, Full Fluted, Hubless072225Silicone Channel Drain (19F) with 4.7mm (3/16") TrocarSilicone Channel Drain, 19F, Round, 0.75 Fluted and packaged with 4.7mm (3/16") Trocar072223Silicone Channel Drain (15 Fr) with TrocarRound, 3/4 fluted drain072221Silicone Channel Drain (15F) with 3.2mm (1/8") TrocarSilicone Channel Drain, 15F, Round, 0.75 Fluted and packaged with 3.2mm (1/8") Trocar072217Silicone Channel Drain (10 mm) with TrocarFlat, 3/4 fluted drain072216Silicone Channel Drain (7mm) with 4.7mm (3/16") TrocarSilicone Channel Drain, 7mm, Flat, Full Fluted and packaged with 4.7mm (3/16") Trocar072215Silicone Channel Drain (10mm) with 4.7mm (3/16") TrocarSilicone Channel Drain, 10mm, Flat, Full Fluted and packaged with 4.7mm (3/16") Trocar072214Silicone Channel Drain (10mm)Silicone Channel Drain, 10mm, Flat, Full Fluted072213Silicone Channel Drain (10 mm)Flat, 3/4 fluted drain072212Silicone Channel Drain (7 mm) with TrocarFlat, full fluted drain072211Silicone Channel Drain (7 mm)Flat, full fluted drain072210Silicone Channel Drain (7mm)Silicone Channel Drain, 7mm, Flat, 0.75 Fluted072192Silicone Channel Drain (19F) with 6.3mm (1/4") TrocarSilicone Channel Drain, 19F, Round, Full Fluted and packaged with 6.3mm (1/4") Trocar072191Silicone Channel Drain (19F) with 4.7mm (3/16") TrocarSilicone Channel Drain, 19F, Round, Full Fluted and packaged with 4.7mm (3/16") Trocar072190Silicone Channel Drain (19F)Silicone Channel Drain, 19F, Round, Full Fluted072189Silicone Channel Drain (15F) with 4.7mm (3/16") TrocarSilicone Channel Drain, 15F, Round, Full Fluted and packaged with 4.7mm (3/16") Trocar072188Silicone Channel Drain (15 Fr)Round, full fluted drain072187Silicone Channel Drain (10F) with 3.2mm (1/8") TrocarSilicone Channel Drain, 10F, Round, Full Fluted and packaged with 3.2mm (1/8") Trocar072186Silicone Channel Drain (10F)Silicone Channel Drain, 10F, Round, Full Fluted0080730PVC Drain, 1/4" (19F) with TrocarDouble round, mid perforated/fluted siliconized PVC round drain with 12 in. hole pattern and radiopaque stripe and packaged with Trocar.0080720PVC Drain, 3/16" (15F) with TrocarDouble round, mid perforated/fluted siliconized PVC round drain with 12 in. hole pattern and radiopaque stripe and packaged with Trocar.0080710PVC Drain, 1/8" (10F) with TrocarDouble round, mid perforated/fluted siliconized PVC round drain with 12 in. hole pattern and radiopaque stripe and packaged with Trocar.0080700PVC Drain, 3/32" (7F) with TrocarDouble round, mid perforated/fluted siliconized PVC round drain with 12 in. hole pattern and radiopaque stripe and packaged with Trocar.0073320Evacuator Kit with Round Silicone drain (15F) and 100cc Bulb EvacuatorEnd Perforated/Fluted, 49" long drain packaged with Trocar0073310Silicone Bulb Evacuator Kit (1/8 in) with TrocarKit includes round, end perforated drain and 100cc Silicone Suction Evacuator0072440Silicone Bulb Evacuator Kit (10 mm) with TrocarKit includes flat-hubless, full perforated drain and 100cc Silicone Suction Evacuator0072430Evacuator Kit with Flat Silicone drain (7mm) and 100cc Bulb EvacuatorFull Perforated/Fluted, 20cm long, Hubless drain packaged with Trocar0072370Silicone Bulb Evacuator Kit (10 mm) with TrocarKit includes hubless, 3/4 perforated drain and 100cc Silicone Suction Evacuator0072360Evacuator Kit with Flat Silicone drain (7mm) and 100cc Bulb Evacuator0.75 Perforated/Fluted, 20cm long, Hubless drain packaged with Trocar0071440Evacuator Kit with Flat Silicone drain (10mm) and 100cc Bulb EvacuatorFull Perforated/Fluted, 20cm long, Hubless drain0071430Silicone Bulb Evacuator Kit (7 mm)Kit includes flat-hubless, full perforated drain and 100cc Silicone Suction Evacuator0071370Silicone Bulb Evacuator Kit (10 mm)Kit includes hubless, 3/4 perforated drain and 100cc Silicone Suction Evacuator0071360Evacuator Kit with Flat Silicone drain (7mm) and 100cc Bulb Evacuator0.75 Perforated/Fluted, 20cm long, Hubless drain0070720Silicone Drain (3/16 in) with TrocarDouble Round, mid perforated drain with a 124.4 cm length0070440Silicone Drain (10 mm)Flat-Hubless, full perforated drain with a 20 cm length0070400Closed Wound Suction Evacuator (400cc)Includes anti-reflux valve0070370Silicone Drain (10 mm)Flat-Hubless, 3/4 perforated drain with a 20 cm length0070310Silicone Drain (1/8 in) with TrocarRound, end perforated drain with a 124.4 cm lenght0070230Silicone Drain (1/4 in)Round, end perforated drain with a 124.4 cm lenght0070220Silicone Drain (3/16 in)Round, end perforated drain with a 124.4 cm lenght0070210Silicone Drain (1/8 in)Round, end perforated drain with a 124.4 cm lenght0070200Silicone Drain (3/32 in)Round, end perforated drain with a 124.4 cm lenght0043670Three Spring Evacuator Kit (1/4 in) with TrocarKit includes round, end perforated drain and 400cc 3-Spring Evacuator with Y-connecting tube0043660Evacuator Kit with Round Silicone drain (10F) and 400cc 3-Spring EvacuatorEnd Perforated/Fluted drain packaged with Trocar and Y-Connector00436503-Spring Evacuator (400cc)Includes Y-connecting tube0043630Evacuator Kit with Round PVC drain (15F) and 400cc 3-Spring EvacuatorEnd Perforated/Fluted drain packaged with Trocar and Y-Connector0043620Evacuator Kit with Round PVC drain (19F) and 400cc 3-Spring EvacuatorEnd Perforated/Fluted drain packaged with Trocar and Y-Connector0043610Three Spring Evacuator Kit (1/8 in) with TrocarKit includes round, mid perforated drain and 400cc 3-Spring Evacuator with Y-connecting tube0043600Three Spring Evacuator Kit (3/32 in) with TrocarKit includes round, mid perforated drain and 400cc 3-Spring Evacuator with Y-connecting tube0034760Stainless Steel Trocar (1/8 in)For use with silicone or PVC0034660PVC Drain (1/8 in)Double round, mid perforated drainwound drains, channel drain, surgical drain, penrose drain, jp drain/en-us/products-and-solutions/products/product-families/bd-wound-drains