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K3Pro Transfer Accessories - Transfer

by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG 18 variants

Ref VBA_OTK50Model Transfer Accessories - Transfer

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

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++EAGNTRANSFERUK Basic UDI-DI EAGNVBAOTK500UDI-DIDate21 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberEAGNVBAOTK500 UDI-DI Date21 Sep 2016ListedStatusListed 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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
K3Pro Transfer Accessories - Transfer EUDAMED
K3Pro Konus Dental Implants GUDID
Generic Name
Dental implant suprastructure, temporary, preformed, reusable
Model / Ref / Catalog
Transfer Accessories - Transfer, VBA_OTK50
Primary DI / UDI-DI
EAGNVBAOTK500
Basic UDI-DI
++EAGNTRANSFERUK
510(k) Number
FDA Product Code
NDP
EMDN Code
P0180 Facial and odontological prostheses - accessories
GMDN Term
Dental implant suprastructure, temporary, preformed, reusable
Device Class
Class I
Regulation Number
872.3980
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
ImplantableEUDAMED
No
GUDID
Yes

Manufacturer details

EUDAMED SRN
DE-MF-000012472

Other devices from Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG

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Properties

  • Implantable NoEUDAMEDYesGUDID
  • Prescription Use
  • Lot / Batch Number

Other properties (21)

  • Sterile: No
  • Single Use: 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
  • Manufacturing Date: No