Endoch DGF-2318A

Endoch DGF-2318A is a Class II device made by Endoch Inc, listed in FDA GUDID since 3 Jun 2019 (UDI-DI DGF23181), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberDGF23181 UDI-DI	Date3 Jun 2019Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Endoch
Generic name: Flexible endoscopic tissue manipulation forceps, reusable
Model / Ref / Catalog: DGF-2318A

Primary DI / UDI-DI: DGF23181
FDA product code: GEI, GEN
GMDN term: Flexible endoscopic tissue manipulation forceps, reusable

Device class: Class II
Regulation number: 878.4400, 878.4800
GUDID distribution status: In Commercial Distribution

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Other devices filed under Flexible endoscopic tissue manipulation forceps, reusable.

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Properties

Supplied sterile
Single use

Other properties (13, all answered No)