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IO Freedom

by Extremity Medical, LLC 14 variants

Ref 147-07045

IO Freedom (147-07045) is a device classified as Class IIa in the EU and Class I in the US made by Extremity Medical, LLC, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI B-00842078129845) and listed in FDA GUDID since 29 Oct 2026 (UDI-DI 00842078129845), active as of 9 Nov 2026.

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

CE MDD

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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00842078129845 Basic UDI-DI 00842078129845UDI-DIDate4 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00842078129845 UDI-DI Date29 Oct 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00842078129845 registered 4 Nov 2026 Active
  • FDA GUDID UDI-DI 00842078129845 listed 29 Oct 2026 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00842078129845
  2. Registered EUDAMED B-00842078129845

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Generic name
Surgical drill guide, reusable
Model / reference
147-07045
Primary DI / UDI-DI
00842078129845 EUDAMED
00842078129784 GUDID
Basic UDI-DI
B-00842078129845
FDA product code
LXH
EMDN code
P091399 Orthopaedic implant instruments, single-use - other
GMDN term
Surgical drill guide, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.4540
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00842078129845
GUDID
00842078129784
Device classEUDAMED
Class IIa
GUDID
Class I
Sterilise before useEUDAMED
No
GUDID
Yes

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00842078129845; FDA GUDID lists 00842078129784), so their flags are not compared. Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Manufacturer details

EUDAMED SRN
US-MF-000018334
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from Extremity Medical, LLC

See all devices from Extremity Medical, LLC →

Properties

  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (18, all answered No)