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Unicen 21

by Álvarez Redondo, S.A.

Ref CE 126IVD, CE 127IVD

Unicen 21 (CE 126IVD) is an in vitro diagnostic device (EU IVDR Class A; EMDN category centrifuges) made by Álvarez Redondo, S.A., registered in EUDAMED on 10 Dec 2024 (Basic UDI-DI 843661198-IVD-UNI1-JZ), 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 Number843661198-IVD-UNI1-JZ Basic UDI-DI Date10 Dec 2024RegisteredStatusActive

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  • Withdrawn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
CE 126IVD, CE 127IVD
Primary DI / UDI-DI
08436611980202, 08436611980219
Basic UDI-DI
843661198-IVD-UNI1-JZ
EMDN code
W02069003 Centrifuges
Device class
Class A
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000000560

Similar devices in this category

Other devices filed under CENTRIFUGES.

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Properties

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