Skip to content

Brucellacapt®

by Vircell, S.L

Ref BRUCAPT

Brucellacapt® (BRUCAPT) is a device classified as IVD General made by Vircell, S.L, registered in EUDAMED on 2 Oct 2026 (Basic UDI-DI B-08436040325773), active as of 25 Oct 2026.

Active European Union

CE IVDD

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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-08436040325773 Basic UDI-DI 08436040325773UDI-DIDate2 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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Model / reference
BRUCAPT
Primary DI / UDI-DI
08436040325773
Basic UDI-DI
B-08436040325773
EMDN code
W0105011701 Brucella
Device class
Class IVD General
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000004099

Similar devices in this category

Other devices filed under OTHER BACTERIOLOGY IMMUNOASSAYS.

Other devices from Vircell, S.L

See all devices from Vircell, S.L →

Properties

  • Contains human tissues or cells
  • Contains animal tissues or cells
  • Contains substances of microbial origin
  • Reagent
  • IVD kit
  • Professional testing
Other properties (6, all answered No)