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Current as of October 02, 2022 | Updated by FindLaw Staff
(a) Identification. A hydrogel wounddressing is a sterile or non- sterile device intended to cover a wound, to absorb wound exudate, to control bleeding or fluid loss, and to protect against abrasion, friction, desiccation, and contamination. It consists of a nonresorbable matrix made of hydrophilic polymers or other material in combination with water (at least 50 percent) and capable of absorbing exudate. This classification does not include a hydrogel wounddressing that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.
(b) Classification. Class I (general controls). The device is exempt from the premarket notification procedures in part 807, subpart E of this chapter subject to the limitations in § 878.9.
Cite this article: FindLaw.com - Code of Federal Regulations Title 21. Food and Drugs § 21.878.4022 Hydrogel wound dressing and burn dressing - last updated October 02, 2022 | https://codes.findlaw.com/cfr/title-21-food-and-drugs/cfr-sect-21-878-4022/
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