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MicroVue Bp Plus EIA

by Quidel Corp.

Ref A027Model MicroVue

MicroVue Bp Plus EIA (A027) is a device classified as IVD General (EU), Class II (US) made by Quidel Corp., registered in EUDAMED on 22 Oct 2026 (Basic UDI-DI B-30014613335573) and listed in FDA GUDID since 16 Sep 2016 (UDI-DI 30014613335573), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE IVDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD EUDAMED NumberB-30014613335573 Basic UDI-DI 30014613335573UDI-DIDate22 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number30014613335573 UDI-DI Date16 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-30014613335573 registered 22 Oct 2026 Active
  • FDA GUDID UDI-DI 30014613335573 listed 16 Sep 2016 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 30014613335573
  2. Registered EUDAMED B-30014613335573

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
MicroVue Bb Plus EIA EUDAMED
MicroVue GUDID
Generic name
Complement component B IVD, kit, enzyme immunoassay (EIA)
Device name
Bb Plus EIA
Model / Ref / Catalog
MicroVue, A027, Bp Plus EIA
Primary DI / UDI-DI
30014613335573
Basic UDI-DI
B-30014613335573
FDA product code
JZH
EMDN code
W0102010204 Complement component for bb
GMDN term
Complement component B IVD, kit, enzyme immunoassay (EIA)
Device class
Class IVD General EUDAMED
Class II GUDID
Regulation number
866.5320
EU registration type
Legacy device (under a directive)
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
MicroVue
A027
GUDID
Bp Plus EIA
Device classEUDAMED
Class IVD General
GUDID
Class II

Device class is stated on each registry's own scale: Class IVD General in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Complement component B IVD, kit, enzyme immunoassay (EIA)

Similar devices in this category

Other devices filed under COMPLEMENT COMPONENTS.

Other devices from Quidel Corp.

See all devices from Quidel Corp. →

Properties

  • Single use
  • Contains animal tissues or cells
  • Reagent
  • IVD kit
  • Professional testing
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (16, all answered No)