M-ORTTL Assembly
M-ORTTL Assembly (317-10275) is a Class I device made by Quality Aspirators, listed in FDA GUDID since 27 Feb 2025 (UDI-DI 00814005024295), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00814005024295 | Date27 Feb 2025 | StatusListed |
Official records
- AccessGUDID record 00814005024295
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Head-worn lamp
- Model / Ref / Catalog
- M-ORTTL Assembly, 317-10275
- Primary DI / UDI-DI
- 00814005024295
- FDA product code
- KYT
- GMDN term
- Head-worn lamp
- Device class
- Class I
- Regulation number
- 880.6350
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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