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Adriamed C ALL.2 Bianca

by Pharmapiu SRL

Ref 6602-BI

Active European Union

CE MDR

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805267959ALL2GR Basic UDI-DI 08052679590728UDI-DIDate27 Oct 2025RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
kit primo sooccorso conforme all.2 D.lgs81
Model / Reference
6602-BI
Primary DI / UDI-DI
08052679590728
Basic UDI-DI
805267959ALL2GR
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
kit primo sooccorso conforme all.2 D.lgs81

Manufacturer details

EUDAMED SRN
IT-PR-000038189

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Properties

Other properties (1)

  • Sterile: No