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Elmed 31540-34

by Elmed Incorporated

Elmed 31540-34 is a Class I device made by Elmed Incorporated, listed in FDA GUDID since 14 Mar 2023 (UDI-DI 00842180149175), 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 Number00842180149175 UDI-DI Date14 Mar 2023ListedStatusListed 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  • Withdrawn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 scissors, reusable
Model / Ref / Catalog
31540-34
Primary DI / UDI-DI
00842180149175
FDA product code
NWW
GMDN term
Flexible endoscopic scissors, reusable
Device class
Class I
Regulation number
884.1690
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Flexible endoscopic scissors, reusable

Similar devices in this category

Other devices filed under Flexible endoscopic scissors, reusable.

Other devices from Elmed Incorporated

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Manufacturing date
Other properties (11, all answered No)