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ART.301.SALVI MEDICALE PODKOLANÓWKI KOMPRESYJNE OTWARTE PALCE Ccl.II STOPIEŃ KOMPRESJI 23-32 mmHg CZARNY ROZMIAR M

by PMT Sp. z o.o.

Ref 301.MEDICALE.CZARNY.M

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 Number590746758MEDICALEMIKROCX Basic UDI-DI 05907467580050UDI-DIDate29 Aug 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  • Withdrawn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
II klasa kompresji Salvi Medicale Mikrofibra
Model / Reference
301.MEDICALE.CZARNY.M
Primary DI / UDI-DI
05907467580050
Basic UDI-DI
590746758MEDICALEMIKROCX
EMDN Code
M030405 Compression stockings
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000032661

Other devices from PMT Sp. z o.o.

See all devices from PMT Sp. z o.o. →

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