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Vitberg Recovery System - Moduł Brzuch RS2 (Moduł rehabilitacyjny V2MFSP)

by Vitberg Sikora Jacek

Ref V2MFSModel Moduł RS2

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number590470340V2MABT Basic UDI-DI 05904703400592UDI-DIDate6 Feb 2024RegisteredStatusActive

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  • Withdrawn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
Moduł RS2
Model / Reference
Moduł RS2, V2MFS
Primary DI / UDI-DI
05904703400592
Basic UDI-DI
590470340V2MABT
Direct Marketing DI
05904703400592
EMDN Code
Z120616 Electromechanical systems for physical therapy
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000010936

From the manufacturer

Manufacturer's product page: Moduł Brzuch Vitberg RS2

Other devices from Vitberg Sikora Jacek

See all devices from Vitberg Sikora Jacek →

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