Uline S-22137
by Uline, Inc.
Uline S-22137 is a Class II device made by Uline, Inc., listed in FDA GUDID since 14 Jun 2018 (UDI-DI 10851253007561), 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 | Number10851253007561 | Date14 Jun 2018 | StatusListed |
Official records
- AccessGUDID record 10851253007561
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Uline
- Generic name
- Surgical/medical face mask, single-use
- Model / Ref / Catalog
- S-22137
- Primary DI / UDI-DI
- 10851253007561
- FDA product code
- FXX
- GMDN term
- Surgical/medical face mask, single-use
- Device class
- Class II
- Regulation number
- 878.4040
- GUDID distribution status
- In Commercial Distribution
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