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BIONIKA BIOPLANT, Multifunkciós fej

by BIONIKA Medline Kft. EUDAMED

Active European Union

Ref 502394041000

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number599322000ST Basic UDI-DIDate20 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Impression devices, Class I.
Model / Reference
502394041000
Primary DI / UDI-DI
05993223094725
Basic UDI-DI
599322000ST
EMDN Code
Q010207 Dental impression devices for prosthetic dentistry
Device Class
Class I
Market of Registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000004631

Other devices from BIONIKA Medline Kft.

See all devices from BIONIKA Medline Kft. →

Properties

  • Reusable

Other properties (12)

  • Sterile: 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No