Skip to content

VeriPlate Set of 10 (10ql)

by Hamilton AG

Ref 10169572

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

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

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number07630032610169572VE Basic UDI-DI 07630032660885UDI-DIDate20 Mar 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Trade Name
VeriPlate Set of 10 (10ql)
VeriPlate
Device Name
VeriPlate Set of 10 (10 µL)
Model / Reference
10169572
Primary DI / UDI-DI
07630032660885
Basic UDI-DI
07630032610169572VE, 76300326101695725F
Direct Marketing DI
07630032660885
EMDN Code
W0580 IVD general use consumables devices - other accessories
Device Class
Class A
EU market of registration
Belgium
Austria

Manufacturer details

EUDAMED SRN
CH-MF-000013585
Authorised representative
Johner Medical GmbH DE-AR-000011832

Other devices from Hamilton AG

See all devices from Hamilton AG →

Properties

  • New Device YesEUDAMEDNoEUDAMED

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No