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Spincare® Kit

by Nanomedic Technologies Ltd.

Ref SLK001

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-(01)07290018270011JG Basic UDI-DI D-(01)07290018270011JGUDI-DIDate6 Aug 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Spincare Kit
Model / Reference
SLK001
Primary DI / UDI-DI
D-(01)07290018270011JG
Basic UDI-DI
B-(01)07290018270011JG
EMDN Code
M040499 Dressings for wounds, sores and ulcerations - other
Device Class
Class IIa
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
IL-MF-000031337
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Nanomedic Technologies Ltd.

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No