CFM Technologies ENT-DMK
CFM Technologies ENT-DMK is a direct ophthalmoscope (FDA Class I) made by C F M Technologies Inc, listed in FDA GUDID since 6 Jan 2020 (UDI-DI 00850013958252), registry data 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 | Number00850013958252 | Date6 Jan 2020 | StatusListed |
Official records
- AccessGUDID record 00850013958252
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- CFM Technologies
- Generic name
- Direct ophthalmoscope
- Model / reference
- ENT-DMK
- Description
- Deluxe ENT Field Corpsman Kit. This kit contains a versatile set of components designed to facilitate effective examination of the eyes, ears, nose and throat.
- Primary DI / UDI-DI
- 00850013958252
- FDA product code
- HPN, JYG, ERA
- GMDN term
- Direct ophthalmoscope
- Device class
- Class I
- Regulation number
- 886.4445, 874.4420, 874.4770
- GUDID distribution status
- In Commercial Distribution
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Other devices filed under FDA product code HPN (Magnet, Permanent).
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- PAREL RARE EARTH MAGNET, I.O.M., INTRAOCULAR MAG by Richard James, Inc.
- EYE SEE INSTRUMENT by King Tool, Inc.