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KONG-TL VBR System, Trial End Plate, rectangular, L, 0° x 43 mm 44-001-00-43

by Icotec

Ref 44-001-00-43Model Trial End Plate

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

CE MDR

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 Number764017255iVBRTL0001XF Basic UDI-DI 07640164847771UDI-DIDate3 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07640164847771 UDI-DI Date19 Jun 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  • Withdrawn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 Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
KONG®-TL VBR System Trial End Plate, rectangular, L <0° ↔ 43 mm EUDAMED
KONG-TL VBR System, Trial End Plate, rectangular, L, 0° x 43 mm GUDID
Generic Name
Surgical implant template, reusable
Model / Ref / Catalog
44-001-00-43, Trial End Plate
Primary DI / UDI-DI
07640164847771
Basic UDI-DI
764017255iVBRTL0001XF
Direct Marketing DI
07640164847771
FDA Product Code
MQP, PLR
EMDN Code
L1109 Neurosurgery and spinal surgery instrument kits, reusable
GMDN Term
Surgical implant template, reusable
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
888.3060
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Category: Surgical implant template, reusable

Other devices from Icotec

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Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: 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
  • Expiration Date: No