SourceMark M0322
by Sourcemark, LLC. 3 variants
SourceMark M0322 is a Class I device made by Sourcemark, LLC., listed in FDA GUDID since 6 Nov 2020 (UDI-DI 00813799007293), 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 | Number00813799007293 | Date6 Nov 2020 | StatusListed |
Official records
- AccessGUDID record 00813799007293
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- SourceMark
- Generic name
- Laryngeal mask airway, single-use
- Model / reference
- M0322
- Primary DI / UDI-DI
- 00813799007293
- FDA product code
- CAE
- GMDN term
- Laryngeal mask airway, single-use
- Device class
- Class I
- Regulation number
- 868.5110
- GUDID distribution status
- In Commercial Distribution
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