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Specimen Collection Container A

by Alfresa Pharma Corporation 6 variants

Ref 914356

Active European Union

CE IVDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number4987274W05019001SCC007Z Basic UDI-DI 04987274143564UDI-DIDate3 Mar 2022RegisteredStatusActive

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  • Withdrawn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
914356
Primary DI / UDI-DI
04987274143564
Basic UDI-DI
4987274W05019001SCC007Z
EMDN Code
W05019001 Faeces collection devices
Device Class
Class A
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
JP-MF-000008778
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Alfresa Pharma Corporation

See all devices from Alfresa Pharma Corporation →

Properties

  • Animal Tissues
  • Reagent

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No