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Akumata Ergonomiczny podnóżek do akupresury, czarno-zielony

by ACUS MED Sp. z o.o.

Ref ERP-005273

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 Number5903900638AKUMATAMW Basic UDI-DI 05905123607196UDI-DIDate8 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

PolandCzech RepublicRomania
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 3 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Czechia since 19 Oct 2026
  • Poland since 19 Oct 2026
  • Romania since 19 Oct 2026

Last checked 25 Oct 2026.

Specification

EUDAMED

Device Name
Zestaw do akupresury
Model / Reference
ERP-005273
Primary DI / UDI-DI
05905123607196
Basic UDI-DI
5903900638AKUMATAMW
Direct Marketing DI
05905123607196
EMDN Code
Z12069099 Various physiotherapy and rehabilitation instruments - other
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000049758

Other devices from ACUS MED Sp. z o.o.

See all devices from ACUS MED 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