Mask 1002250
Mask 1002250 is a Class I device made by Westmed, Inc., listed in FDA GUDID since 31 Mar 2022 (UDI-DI 00709078014291), 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 | Number00709078014291 | Date31 Mar 2022 | StatusListed |
Official records
- AccessGUDID record 00709078014291
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Mask
- Generic name
- Aerosol face mask, non-rebreathing
- Model / reference
- 1002250
- Description
- Mask Adult Aerosol (Vented)
- Primary DI / UDI-DI
- 00709078014291
- FDA product code
- BYG
- GMDN term
- Aerosol face mask, non-rebreathing
- Device class
- Class I
- Regulation number
- 868.5580
- GUDID distribution status
- In Commercial Distribution
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