Endoch DHB-2323OF
by Endoch Inc
Endoch DHB-2323OF is a Class I device made by Endoch Inc, listed in FDA GUDID since 1 Jun 2019 (UDI-DI DHB232343), 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 | NumberDHB232343 | Date1 Jun 2019 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Endoch
- Generic name
- Flexible endoscopic biopsy forceps, single-use
- Model / Ref / Catalog
- DHB-2323OF
- Primary DI / UDI-DI
- DHB232343
- FDA product code
- HFB, FCL
- GMDN term
- Flexible endoscopic biopsy forceps, single-use
- Device class
- Class I
- Regulation number
- 884.4530, 876.1075
- GUDID distribution status
- In Commercial Distribution
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