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Medfix

by Medfix International, LLC 15 variants

Part of a family of 20 devices: see the family page

Ref MF-0112LModel Retractor Frame

Medfix (MF-0112L) is a Class I device made by Medfix International, LLC, registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 081002183RETRACTORFRAME54), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number081002183RETRACTORFRAME54 Basic UDI-DI 00850061673596UDI-DIDate28 Oct 2026RegisteredStatusActive

Official records

  • EUDAMED public site Basic UDI-DI 081002183RETRACTORFRAME54 — open Devices and search for it

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Retractor Frame, MF-0112L
Primary DI / UDI-DI
00850061673596
Basic UDI-DI
081002183RETRACTORFRAME54
Direct marketing DI
00850061673596
EMDN code
L11050199 Vertebral surgery spreaders and retractors, reusable - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000053473
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Similar devices in this category

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

Other devices from Medfix International, LLC

See all devices from Medfix International, LLC →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)