PremierPro 3771
PremierPro 3771 is a Class I device made by Prestige Ameritech, listed in FDA GUDID since 26 Aug 2020 (UDI-DI 00811220032364), registry data as of 22 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 | Number00811220032364 | Date26 Aug 2020 | StatusListed |
Official records
- AccessGUDID record 00811220032364
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PremierPro
- Generic name
- Absorbent underpad, non-antimicrobial, single-use
- Model / Ref / Catalog
- 3771
- Description
- Underpad XL Premium, 40" x 59", White, 5/bg SIP Breathable Underpad, REMUV 36"x60" 5/bg
- Primary DI / UDI-DI
- 00811220032364
- FDA product code
- KME
- GMDN term
- Absorbent underpad, non-antimicrobial, single-use
- Device class
- Class I
- Regulation number
- 880.6060
- GUDID distribution status
- In Commercial Distribution
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