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Elmed 31340-23

by Elmed Incorporated

Elmed 31340-23 is a Class I device made by Elmed Incorporated, listed in FDA GUDID since 1 Jul 2024 (UDI-DI 00198506059322), 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 Number00198506059322 UDI-DI Date1 Jul 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Elmed
Generic name
Flexible endoscopic tissue manipulation forceps, reusable
Model / Ref / Catalog
31340-23
Primary DI / UDI-DI
00198506059322
FDA product code
KOA
GMDN term
Flexible endoscopic tissue manipulation forceps, reusable
Device class
Class I
Regulation number
876.4730
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Flexible endoscopic tissue manipulation forceps, reusable

Similar devices in this category

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

Other devices from Elmed Incorporated

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)