Kimberly-Clark announced that it is the first and only manufacturer to receive 510(k) clearance from the U.S. Food and Drug Administration (FDA) for use of the KIMGUARD ONE-STEP Sterilization Wrap portfolio with all Advanced Sterilization Products (ASP) STERRAD Systems, including the new DUO Cycle for the STERRAD 100NX System.
Kimberly-Clark announced that it is the first and only manufacturer to receive 510(k) clearance from the U.S. Food and Drug Administration (FDA) for #
As always, users can continue to have confidence that their instruments wrapped with KIMGUARD ONE-STEP Sterilization Wrap, which includes KIMGUARD ONE-STEP Quick Check, will maintain sterility of the enclosed medical instruments until used. The ONE-STEP Sterilization Wrap is cleared for use with all major sterilization modalities: STERRAD Sterilization Systems, Pre-vacuum Steam, Ethylene Oxide (EO) and Amsco V-Pro.
Kimberly-Clark announced that it is the first and only manufacturer to receive 510(k) clearance from the U.S. Food and Drug Administration (FDA) for #
"Surgical sterilization technology is rapidly evolving and, as an innovator in the market, we have worked closely with ASP and FDA to obtain clearance of the KIMGUARD ONE-STEP Sterilization Wrap now qualified for use with all STERRAD Systems," said Steve Camp, Vice President, Regulatory and Clinical Affairs, Kimberly-Clark Health Care.
Kimberly-Clark announced that it is the first and only manufacturer to receive 510(k) clearance from the U.S. Food and Drug Administration (FDA) for #
"Thorough testing and evaluation of the KIMGUARD family of Sterilization Wrap products with all available sterilization processing modalities are paramount to sterility assurance. Kimberly-Clark is pleased to provide clinicians with this added assurance of sterility of their instruments supporting their mission of delivering excellent patient care."
Kimberly-Clark announced that it is the first and only manufacturer to receive 510(k) clearance from the U.S. Food and Drug Administration (FDA) for #
KIMGUARD Sterilization Wrap meets the most rigorous industry standards for safety and performance, including resistance to fire, abrasion, and microbial contamination, to maintain the sterility of instruments.
Kimberly-Clark announced that it is the first and only manufacturer to receive 510(k) clearance from the U.S. Food and Drug Administration (FDA) for #
"Advanced Sterilization Products' STERRAD Systems represents the largest installed base of hydrogen peroxide sterilization systems throughout the world," said Anthony Bishop, Vice President, Global Marketing, ASP. "With the growing importance of having the manufacturers' instructions for use (IFUs) support the sterilization system, this new update will help ensure the safest possible environment for patients and their families, healthcare workers, providers and communities."
Kimberly-Clark announced that it is the first and only manufacturer to receive 510(k) clearance from the U.S. Food and Drug Administration (FDA) for #
About Kimberly-Clark
Kimberly-Clark Corp. and its well-known global brands are an indispensable part of life for people in more than 175 countries. Every day, nearly a quarter of the world's population trust K-C's brands and the solutions they provide to enhance their health, hygiene and well-being. With brands such as Kleenex, Scott, Huggies, Pull-Ups, Kotex and Depend, Kimberly-Clark holds the No. 1 or No. 2 share position in more than 80 countries.
Kimberly-Clark announced that it is the first and only manufacturer to receive 510(k) clearance from the U.S. Food and Drug Administration (FDA) for #
Kimberly Clark
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