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Vibra 3.0

by Ad Swiss Medtech SA Switzerland EUDAMED

Ref DP001Model DP001 Vibra 3.0

EMDN Z12062899

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7649990376DP001FW Basic UDI-DIDate17 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
DP001 Vibra 3.0
Model / Reference
DP001 Vibra 3.0, DP001
Primary DI / UDI-DI
07649990376011
Basic UDI-DI
7649990376DP001FW
Direct Marketing DI
07649990376011
EMDN Code
Z12062899 Neuromuscular stimulation equipment - other
Device Class
Class IIa
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
CH-MF-000037918
Authorised representative
DO WELL TECHNOLOGIES DI BUCCI CLAUDIA IT-AR-000029315

Other devices from Ad Swiss Medtech SA

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED ac61c67f-53ba-48fd-936b-c068ed770a23 61 fields · synced 22 Oct 2026