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Medfix MF-2335BLS

by Medfix International, LLC

Ref MF-2335BLSModel Retractor Blades

Medfix MF-2335BLS is a Class I device made by Medfix International, LLC, registered in EUDAMED on 17 Sep 2026 (Basic UDI-DI 081002183RETRACTORBLADEZG) and listed in FDA GUDID since 3 Apr 2020 (UDI-DI 00810021834498), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number081002183RETRACTORBLADEZG Basic UDI-DI 00810021834498UDI-DIDate17 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00810021834498 UDI-DI Date3 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 081002183RETRACTORBLADEZG registered 17 Sep 2026 Active
  • FDA GUDID UDI-DI 00810021834498 listed 3 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00810021834498
  2. Registered EUDAMED 081002183RETRACTORBLADEZG

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  • Withdrawn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
Medfix
Generic name
Surgical retractor/retraction system blade, reusable
Model / reference
MF-2335BLS, Retractor Blades
Primary DI / UDI-DI
00810021834498
Basic UDI-DI
081002183RETRACTORBLADEZG
Direct marketing DI
00810021834498
FDA product code
MDM
EMDN code
L11050199 Vertebral surgery spreaders and retractors, reusable - other
GMDN term
Surgical retractor/retraction system blade, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical retractor/retraction system blade, reusable

Similar devices in this category

Other devices filed under VERTEBRAL SURGERY SPREADERS AND RETRACTORS, REUSABLE.

Other devices from Medfix International, LLC

See all devices from Medfix International, LLC →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)