Skip to content

Endoch DBF-2318F

by Endoch Inc

Endoch DBF-2318F is a Class I device made by Endoch Inc, listed in FDA GUDID since 1 Jun 2019 (UDI-DI DBF23183), 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 NumberDBF23183 UDI-DI Date1 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  • Withdrawn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
DBF-2318F
Primary DI / UDI-DI
DBF23183
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

Related devices

Category: Flexible endoscopic biopsy forceps, single-use

Similar devices in this category

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

Other devices from Endoch Inc

See all devices from Endoch Inc →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
Other properties (12, all answered No)