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Zeus Wave

by Wever Instruments. Co., Ltd. South Korea EUDAMED

Ref ZW-IFU-01Model Zeus Wave(Piezo-Type+Pneumatic-Type)

EMDN Z12139001

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800066600082 Basic UDI-DIDate21 Mar 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Zeus Wave(Piezo-Type+Pneumatic-Type)
Model / Reference
Zeus Wave(Piezo-Type+Pneumatic-Type), ZW-IFU-01
Primary DI / UDI-DI
08800066600082
Basic UDI-DI
B-08800066600082
EMDN Code
Z12139001 Shock wave therapy equipment
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
KR-MF-000008615
Authorised representative
Advena Limited MT-AR-000000234

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • 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

Sources (1)

  • EUDAMED 4750ab8c-a9bd-41a2-bebc-cc8a70c82a0d 61 fields · synced 22 Oct 2026