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Vidi Pharma

by Aso Philippines, Inc. 12 variants

Ref NMD-815296Model 39-0446 / 39-0449

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number48079990API07805722 Basic UDI-DI 07071053001149UDI-DIDate8 Oct 2026RegisteredStatusActive

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  • Withdrawn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
Finger Plaster Mix
Model / Reference
39-0446 / 39-0449, NMD-815296
Primary DI / UDI-DI
07071053001149
Basic UDI-DI
48079990API07805722
EMDN Code
M0599 Medical plasters - other
Device Class
Class I
EU market of registration
Norway

Manufacturer details

EUDAMED SRN
PH-MF-000027714
Authorised representative
Aso Europe BV NL-AR-000004377

Other devices from Aso Philippines, Inc.

See all devices from Aso Philippines, Inc. →

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