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VerticaPRO

by Ohh-Med Medical Ltd. Israel EUDAMED

Ref OH_Prod0003

EMDN Z12169004

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7290018772VerticaProEQ Basic UDI-DIDate25 May 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
VerticaPRO
Model / Reference
OH_Prod0003
Primary DI / UDI-DI
07290018772003
Basic UDI-DI
7290018772VerticaProEQ
Direct Marketing DI
07290018772003
EMDN Code
Z12169004 Erectile dysfunction stimulators
Device Class
Class IIa
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
IL-MF-000047353
Authorised representative
G&D&Y NL-AR-000013751

Other devices from Ohh-Med Medical Ltd.

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 f7d5df15-7442-4452-817a-7f556601a62e 61 fields · synced 22 Oct 2026