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Endoch DHB-2323FS

by Endoch Inc

Endoch DHB-2323FS is a Class I device made by Endoch Inc, listed in FDA GUDID since 3 Jun 2019 (UDI-DI DHB232336), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberDHB232336 UDI-DI Date3 Jun 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Endoch
Generic name
Flexible endoscopic biopsy forceps, single-use
Model / Ref / Catalog
DHB-2323FS
Primary DI / UDI-DI
DHB232336
FDA product code
FCL
GMDN term
Flexible endoscopic biopsy forceps, single-use
Device class
Class I
Regulation number
876.1075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Flexible endoscopic biopsy forceps, single-use

Similar devices in this category

Other devices filed under Flexible endoscopic biopsy forceps, single-use.

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Properties

  • Supplied sterile
  • Single use
Other properties (13, all answered No)