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Endoch EAI-0503

by Endoch Inc 2 variants

Endoch EAI-0503 is a Class II device made by Endoch Inc, listed in FDA GUDID since 1 Jun 2019 (UDI-DI EAI0503), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberEAI0503 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  • Withdrawn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
Rigid endoscopic grasping forceps, single-use
Model / Ref / Catalog
EAI-0503
Primary DI / UDI-DI
EAI0503
FDA product code
GEI, GEN
GMDN term
Rigid endoscopic grasping forceps, single-use
Device class
Class II
Regulation number
878.4400, 878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid endoscopic grasping forceps, single-use

Similar devices

Other devices filed under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories).

Other devices from Endoch Inc

See all devices from Endoch Inc →

Properties

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