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VP2000

by Abbott Molecular Inc. 12 variants

Part of a family of 20 devices: see the family page

Ref 02J11-089

VP2000 (02J11-089) is a Class A device made by Abbott Molecular, registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 0884999VyJ0211Q2), 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 Number0884999VyJ0211Q2 Basic UDI-DI 00884999047013UDI-DIDate28 Oct 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  • Withdrawn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

Device name
Abbott VP2000 Processor
Model / reference
02J11-089
Primary DI / UDI-DI
00884999047013
Basic UDI-DI
0884999VyJ0211Q2
EMDN code
W02039004 Automated slide preparation units
Device class
Class A
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000017776
Authorised representative
Abbott GmbH DE-AR-000009457

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Properties

  • Professional testing
  • IVD instrument
Other properties (11, all answered No)