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IVD Sample Collection Kit

by RDA Spot, UAB 57 variants

Ref AVEABT

IVD Sample Collection Kit (AVEABT) is a Class A device made by Rda Spot, Uab, registered in EUDAMED on 21 May 2026 (Basic UDI-DI 477905472AVEABTLZ), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number477905472AVEABTLZ Basic UDI-DI 04779054720641UDI-DIDate21 May 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  • Withdrawn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
AVEABT
Primary DI / UDI-DI
04779054720641
Basic UDI-DI
477905472AVEABTLZ
Direct marketing DI
04779054720641
EMDN code
W0501010199, W0501010299
Device class
Class A
EU registration type
Standard device
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
LT-MF-000027300

Similar devices in this category

Other devices filed under VENOUS OR ARTERIOUS BLOOD COLLECTION DEVICES - OTHER.

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Properties

  • IVD kit
Other properties (12, all answered No)