Altair SA QED-1201
by Qed, Inc.
Altair SA QED-1201 is a Class II device made by Qed, Inc., listed in FDA GUDID since 21 May 2025 (UDI-DI 00860013851538), 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 | Number00860013851538 | Date21 May 2025 | StatusListed |
Official records
- AccessGUDID record 00860013851538
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Altair SA
- Generic name
- Head-worn fibreoptic light
- Model / reference
- QED-1201
- Primary DI / UDI-DI
- 00860013851538
- FDA product code
- FCT
- GMDN term
- Head-worn fibreoptic light
- Device class
- Class II
- Regulation number
- 886.4335
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code FCT (Headlight, Fiberoptic Focusing).
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- MODIFIED SITE FIBER OPTIC MODULE FOR OPHTHAL. USE by Site Microsurgical Systems, Inc.
- Modified Site Fiber Optic Module by Chiron Vision Corp.
- LIGHT COMMANDER by Scieran Technologies, Inc.