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Elmed ST3341525

by Elmed Incorporated

Elmed ST3341525 is a Class I device made by Elmed Incorporated, listed in FDA GUDID since 25 Apr 2024 (UDI-DI 00198506003967), 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 Number00198506003967 UDI-DI Date25 Apr 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  • Withdrawn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
Bone holding forceps
Model / Ref / Catalog
ST3341525
Primary DI / UDI-DI
00198506003967
FDA product code
LXH
GMDN term
Bone holding forceps
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone holding forceps

Similar devices in this category

Other devices filed under Bone holding forceps.

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)