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Elmed ST3153481

by Elmed Incorporated

Elmed ST3153481 is a Class I device made by Elmed Incorporated, listed in FDA GUDID since 24 Apr 2024 (UDI-DI 00198506002540), 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 Number00198506002540 UDI-DI Date24 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  • Withdrawn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
Flexible endoscopic scissors, reusable
Model / Ref / Catalog
ST3153481
Primary DI / UDI-DI
00198506002540
FDA product code
KOA
GMDN term
Flexible endoscopic scissors, 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 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
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)