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Tools - WFS (C) BRT (C)

by Trimed, INC.

Tools - WFS (C) BRT (C) is a Class I device made by Trimed, INC., listed in FDA GUDID since 7 Sep 2016 (UDI-DI 00842188114687), 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 Number00842188114687 UDI-DI Date7 Sep 2016ListedStatusListed 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  • Withdrawn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
Tools - WFS (C)
Generic name
Orthopaedic bone-reduction tool
Model / Ref / Catalog
BRT (C)
Primary DI / UDI-DI
00842188114687
FDA product code
LXH
GMDN term
Orthopaedic bone-reduction tool
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic bone-reduction tool

Similar devices in this category

Other devices filed under Orthopaedic bone-reduction tool.

Other devices from Trimed, INC.

See all devices from Trimed, INC. →

Properties

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