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icotec Lumbar Cage PLIF 4° / 25 mm x 07 mm 12-59-42507

by Icotec

Ref 12-59-42507Model Lumbar Cage PLIF

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

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-07640140433943 Basic UDI-DI 07640140433943UDI-DIDate3 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07640140433943 UDI-DI Date27 Feb 2024ListedStatusListed 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  • Withdrawn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/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
icotec Lumbar Cage, PLIF, <4° ↔ 25 mm ↕ 07 mm EUDAMED
icotec Lumbar Cage PLIF 4° / 25 mm x 07 mm GUDID
Generic Name
Polymeric spinal interbody fusion cage
Model / Ref / Catalog
12-59-42507, Lumbar Cage PLIF
Primary DI / UDI-DI
07640140433943
Basic UDI-DI
B-07640140433943
FDA Product Code
MAX
EMDN Code
P09070101 Spinal cages
GMDN Term
Polymeric spinal interbody fusion cage
Device Class
Class IIb EUDAMED
Class II GUDID
Regulation Number
888.3080
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIb
GUDID
Class II

Related devices

Category: Polymeric spinal interbody fusion cage

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (16)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No