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Pionizator statyczny SMART PRO

by Akces-Med Spółka Z Ograniczoną Odpowiedzialnością

Ref SMDPRO

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59038165SMDPROVE Basic UDI-DI Date12 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  • Withdrawn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

Model / Reference
SMDPRO
Primary DI / UDI-DI
05903816554895, 05903816549648, 05903816551733, 05903816551757, 05903816547972, 05903816545039, 05903816551740, 05903816547828, 05903816547811, 05903816547989, 05903816547835
Basic UDI-DI
59038165SMDPROVE
Direct Marketing DI
05903816554895
05903816549648
05903816551733
05903816551757
05903816547972
05903816545039
05903816551740
05903816547828
05903816547811
05903816547989
05903816547835
EMDN Code
Y050202 Standing frames
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000003624

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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