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Endoch EAI-0710

by Endoch Inc

Endoch EAI-0710 is a Class I device made by Endoch Inc, listed in FDA GUDID since 1 Jun 2019 (UDI-DI EAI0710), 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 NumberEAI0710 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  • Withdrawn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-0710
Primary DI / UDI-DI
EAI0710
FDA product code
GEN, GEI
GMDN term
Rigid endoscopic grasping forceps, single-use
Device class
Class I
Regulation number
878.4800, 878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid endoscopic grasping forceps, single-use

Similar devices

Other devices filed under FDA product code GEN (Forceps, General & Plastic Surgery).

Other devices from Endoch Inc

See all devices from Endoch Inc →

Properties

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