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Pionizator go.spider

by MyWam Sp. z o.o. EUDAMED

Withdrawn No longer placed on the EU market

Ref SPModel Pionizator

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5901122279pionizator2R Basic UDI-DIDate8 Jun 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Model / Reference
Pionizator, SP
Primary DI / UDI-DI
05901122279310
Basic UDI-DI
5901122279pionizator2R
EMDN Code
Y050202 Standing frames
Device Class
Class I

Manufacturer details

EUDAMED SRN
PL-MF-000019252

From the manufacturer

Manufacturer's product page: Pionizator go.spider 1 wzrost użytkownika: 100 – 135 cm max. waga użytkownika: 35 kg Zobacz

Other devices from MyWam Sp. z o.o.

See all devices from MyWam 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