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Masca faciala FFP2 - Adulti - 10 buc

by Intercapital SRL

Ref AKESO10B

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5944759068MASTIMEDICALEN8 Basic UDI-DI 05944759068001UDI-DIDate22 Jun 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Medical use face masks, type II and IIR
Model / Reference
AKESO10B
Primary DI / UDI-DI
05944759068001
Basic UDI-DI
5944759068MASTIMEDICALEN8
EMDN Code
T020603 Medical use face masks, type i (not for healthcare professionals)
Device Class
Class I
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
RO-MF-000024139

From the manufacturer

Manufacturer's product page: Reducere!

Other devices from Intercapital SRL

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No