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Generic Instruments BRT

by Trimed, INC.

Ref BRTModel Reusable Surgical Instruments and Trays

Generic Instruments BRT is a Class I device made by Trimed, INC., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI 08421881BRTV8) and listed in FDA GUDID since 7 Sep 2016 (UDI-DI 00842188110009), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08421881BRTV8 Basic UDI-DI 00842188110009UDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00842188110009 UDI-DI Date7 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08421881BRTV8 registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI 00842188110009 listed 7 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00842188110009
  2. Registered EUDAMED 08421881BRTV8

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Reusable Surgical Instruments and Trays EUDAMED
Generic Instruments GUDID
Generic name
Orthopaedic bone-reduction tool
Model / Ref / Catalog
BRT, Reusable Surgical Instruments and Trays
Primary DI / UDI-DI
00842188110009
Basic UDI-DI
08421881BRTV8
FDA product code
LXH
EMDN code
L0922 Orthopaedic surgery guides, reusable
GMDN term
Orthopaedic bone-reduction tool
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Ireland
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 SURGERY GUIDES, REUSABLE.

Other devices from Trimed, INC.

See all devices from Trimed, INC. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)