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QuikRead Plungers

by Aidian Oy

Ref 67966

QuikRead Plungers (67966) is a Class A device made by Aidian Oy, registered in EUDAMED on 18 May 2022 (Basic UDI-DI 6438115QRPlungersA7), active as of 22 Oct 2026.

Active European Union

CE IVDR

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number6438115QRPlungersA7 Basic UDI-DI 06438115001188UDI-DIDate18 May 2022RegisteredStatusActive

Official records

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  • Withdrawn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

Model / reference
67966
Primary DI / UDI-DI
06438115001188
Basic UDI-DI
6438115QRPlungersA7
EMDN code
W0501010280 Capillary blood collection devices - accessories
Device class
Class A
EU registration type
Standard device
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000023611

Similar devices in this category

Other devices filed under CAPILLARY BLOOD COLLECTION DEVICES.

Other devices from Aidian Oy

See all devices from Aidian Oy →

Properties

  • Near-patient testing
  • Professional testing
Other properties (11, all answered No)