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Inion FreedomScrew™ instrumentation

by Inion Oy

Ref IFS-9052

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

CE MDR CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED NumberB-06438408004070 Basic UDI-DI 06438408004070UDI-DIDate29 Dec 2021RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-06438408004070 Basic UDI-DI 06438408004070UDI-DIDate29 Dec 2021RegisteredStatusActive
United StatesGUDID listing GUDID Number06438408004070 UDI-DI Date8 May 2020ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Inion FreedomScrew™ instrumentation EUDAMED
Inion Universal Instruments EUDAMED
Inion FreedomScrew instruments GUDID
Generic Name
Medical ruler, reusable
Device Name
Inion FreedomScrew instrument
Inion Instruments
Model / Ref / Catalog
IFS-9052, 1
Primary DI / UDI-DI
06438408004070
Basic UDI-DI
B-06438408004070, 6438408INION-IM-INSTRUM68
Secondary DI
M224IFS90529
Direct Marketing DI
06438408004070
FDA Product Code
LXH
EMDN Code
L091002, V0380
GMDN Term
Medical ruler, reusable
Device Class
Class I
Regulation Number
888.4540
EU market of registration
Finland
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
IFS-9052
GUDID
1

Manufacturer details

EUDAMED SRN
FI-MF-000000646

Related devices

Category: Wire holding/twisting forceps

Other devices from Inion, Ltd.

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Properties

  • Reusable
  • Measuring Function
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (18)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No