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Revvity 226 Sample Collection Device

by Wallac Oy 2 variants

Ref GR2265077

Revvity 226 Sample Collection Device (GR2265077) is a Class A device made by Wallac Oy, registered in EUDAMED on 13 Aug 2026 (Basic UDI-DI 6438147GR226SU), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number6438147GR226SU Basic UDI-DI 06438147416028UDI-DIDate13 Aug 2026RegisteredStatusActive

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  • Withdrawn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
GR2265077
Primary DI / UDI-DI
06438147416028
Basic UDI-DI
6438147GR226SU
EMDN code
W0501010299 Capillary blood collection devices - other
Device class
Class A
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
FI-MF-000022620

Similar devices in this category

Other devices filed under CAPILLARY BLOOD COLLECTION DEVICES - OTHER.

Other devices from Wallac Oy

See all devices from Wallac Oy →

Properties

  • Professional testing
  • New device
Other properties (11, all answered No)