Natus RETCAM-FA-UPGRADE
by Xltek
Natus RETCAM-FA-UPGRADE is a Class II device made by Xltek, listed in FDA GUDID since 22 Jun 2021 (UDI-DI 00382830060110), not in commercial distribution (GUDID) 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 | Number00382830060110 | Date22 Jun 2021 | StatusListed |
Official records
- AccessGUDID record 00382830060110
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Natus
- Generic name
- Ophthalmic fundus camera
- Model / reference
- RETCAM-FA-UPGRADE
- Primary DI / UDI-DI
- 00382830060110
- FDA product code
- HKI
- GMDN term
- Ophthalmic fundus camera
- Device class
- Class II
- Regulation number
- 886.1120
- GUDID distribution status
- Not in Commercial Distribution
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