V1274-75 USP Class VI Biocompatibility O-ring
Meets requirements of USP Class VI systemic toxicity, intracutaneous injection and muscle implantation studies:
Today’s constant advancements in medical technology present a plethora of sealing challenges in the life sciences industry. The most critical concern normally faced in medical technology is the purity of a seal.
While some medical applications may never touch human tissue or fluids, deeming standard material selection as appropriate, more critical applications require elastomers to be manufactured and packaged with the utmost “clean” care.
In some instances, seals can react with tissue or fluid causing impurities to leach out of the seal. For this reason, engineers require materials like V1274-75 with few if any impurities.
Product Highlights:
- Good steam resistance for sterilization cycles
- USP Class VI biocompatibility
- FDA compliant
Meets requirements of USP Class VI systemic toxicity, intracutaneous injection and muscle implantation studies:
Today’s constant advancements in medical technology present a plethora of sealing challenges in the life sciences industry. The most critical concern normally faced in medical technology is the purity of a seal.
While some medical applications may never touch human tissue or fluids, deeming standard material selection as appropriate, more critical applications require elastomers to be manufactured and packaged with the utmost “clean” care.
In some instances, seals can react with tissue or fluid causing impurities to leach out of the seal. For this reason, engineers require materials like V1274-75 with few if any impurities.
Benefits:
- Good steam resistance for sterilization cycles
- USP Class VI biocompatibility
- FDA compliant
- Low extractables
- Temperature range of -15 to 400°F
- Low compression se
Recommended For:
- Pharmaceutical processing
- Steam sterilizers
- Disposable and repeat medical device sterilizationa
V1274-75
Elastomers selected for critical applications must consist of “clean” ingredients. These ingredients are outlined by the United States Pharmacopeia (USP), the official standard setting authority on health care products manufactured and distributed in the U.S.A. USP Class VI states that compounds must consist of ingredients with clear histories of biocompatibility and meet tighter requirements for leachables.
Parker’s V1274-75 , primarily developed for pharmaceutical processing, meets the requirements of USP Class VI systemic toxicity, intracutaneous injection and muscle implantation studies. This fluorocarbon material provides good steam resistance for sterilization cycles, USP Class VI biocompatibility, FDA status, low extractables (all of which reduce the risk of contaminating a customer’s product) and good compression set (long life in application / reduced maintenance costs). While V1274-75’s primary application is in pharmaceutical processing, it can also be used in both steam sterilizers and disposable/repeat medical device sterilization.
This warranty comprises the sole and entire warranty pertaining to items provided hereunder. seller makes no other warranty, guarantee, or representation of any kind whatsoever. All other warranties, including but not limited to, merchant ability and fitness for purpose, whether expressed, implied, or arising by operation of law, trade usage, or course of dealing are hereby disclaimed. Notwithstanding the foregoing, there are no warranties whatsoever on items built or acquired wholly or partially, to buyer’s designs or specifications.
Limitation of remedy: Seller’s Liability arising from or in any way connected with the items sold or this contract shall be limited exclusively to repair or replacement of the items sold or refund of the purchase price paid by buyer, at seller’s sole option. In no event shall seller be liable for any incidental, consequential or special damages of any kind or nature whatsoever, including but not limited to lost profits arising from or in any way connected with this agreement or items sold hereunder, whether alleged to arise from breach of contract, expressed or implied warranty, or in tort, including without limitation, negligence, failure to warn or strict liability.
- Details
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Meets requirements of USP Class VI systemic toxicity, intracutaneous injection and muscle implantation studies:
Today’s constant advancements in medical technology present a plethora of sealing challenges in the life sciences industry. The most critical concern normally faced in medical technology is the purity of a seal.
While some medical applications may never touch human tissue or fluids, deeming standard material selection as appropriate, more critical applications require elastomers to be manufactured and packaged with the utmost “clean” care.
In some instances, seals can react with tissue or fluid causing impurities to leach out of the seal. For this reason, engineers require materials like V1274-75 with few if any impurities.
Benefits:
- Good steam resistance for sterilization cycles
- USP Class VI biocompatibility
- FDA compliant
- Low extractables
- Temperature range of -15 to 400°F
- Low compression se
- Specs
-
Recommended For:
- Pharmaceutical processing
- Steam sterilizers
- Disposable and repeat medical device sterilizationa
V1274-75Elastomers selected for critical applications must consist of “clean” ingredients. These ingredients are outlined by the United States Pharmacopeia (USP), the official standard setting authority on health care products manufactured and distributed in the U.S.A. USP Class VI states that compounds must consist of ingredients with clear histories of biocompatibility and meet tighter requirements for leachables.
Parker’s V1274-75 , primarily developed for pharmaceutical processing, meets the requirements of USP Class VI systemic toxicity, intracutaneous injection and muscle implantation studies. This fluorocarbon material provides good steam resistance for sterilization cycles, USP Class VI biocompatibility, FDA status, low extractables (all of which reduce the risk of contaminating a customer’s product) and good compression set (long life in application / reduced maintenance costs). While V1274-75’s primary application is in pharmaceutical processing, it can also be used in both steam sterilizers and disposable/repeat medical device sterilization.
- Resources
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- Warranty
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This warranty comprises the sole and entire warranty pertaining to items provided hereunder. seller makes no other warranty, guarantee, or representation of any kind whatsoever. All other warranties, including but not limited to, merchant ability and fitness for purpose, whether expressed, implied, or arising by operation of law, trade usage, or course of dealing are hereby disclaimed. Notwithstanding the foregoing, there are no warranties whatsoever on items built or acquired wholly or partially, to buyer’s designs or specifications.
Limitation of remedy: Seller’s Liability arising from or in any way connected with the items sold or this contract shall be limited exclusively to repair or replacement of the items sold or refund of the purchase price paid by buyer, at seller’s sole option. In no event shall seller be liable for any incidental, consequential or special damages of any kind or nature whatsoever, including but not limited to lost profits arising from or in any way connected with this agreement or items sold hereunder, whether alleged to arise from breach of contract, expressed or implied warranty, or in tort, including without limitation, negligence, failure to warn or strict liability.
