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Magneto CARE

by Iskra Medical, d.o.o., raziskave in razvoj na področju medicinske opreme in kozmetike

Ref MS022Model 31 Models from MDR Certificate 2023-MDR/QS-009/D

Active European Union

CE MDR

Valid until

15 May 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier 3EC International a.s.

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 Number2023-MDR/QS-009/D Date15 May 2026IssuedStatusActive expires 15 May 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2023-MDR/QS-009/D Active Reissued

    Quality management system EU MDR

    Certifier
    3EC International a.s. 2265
    Issued
    15 May 2026
    Expires
    15 May 2031

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Medical devices for Magneto Therapy
Model / Reference
31 Models from MDR Certificate 2023-MDR/QS-009/D, MS022
Primary DI / UDI-DI
03830066952114
Basic UDI-DI
383006695FMSJ5
Direct Marketing DI
03830066952114
EMDN Code
Z120606 Magnetotherapy equipment
Device Class
Class IIa
EU market of registration
Slovenia

Manufacturer details

EUDAMED SRN
SI-MF-000006345

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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