Remedy MSCWH219S
Remedy MSCWH219S is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 24 Oct 2024 (UDI-DI 10193489009460), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10193489009460 | Date24 Oct 2024 | StatusListed |
Official records
- AccessGUDID record 10193489009460
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Remedy
- Generic name
- Antimicrobial skin friction/moisture control fabric, single-patient reusable
- Model / Ref / Catalog
- MSCWH219S
- Primary DI / UDI-DI
- 10193489009460
- FDA product code
- FRL
- GMDN term
- Antimicrobial skin friction/moisture control fabric, single-patient reusable
- Device class
- Class I
- Regulation number
- 880.5300
- GUDID distribution status
- In Commercial Distribution
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