Identity
- Trade Name
- Pelva Master Kegel Exercise Device EUDAMED
- Device Name
- Pelva Master Kegel Exercise Device EUDAMED
- Model / Reference
- Ves-263 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08964003967079 EUDAMED
- Basic UDI-DI
- 8964003967Ves-263H5 EUDAMED
- EMDN Code
- U070399 PELVIC FLOOR REHABILITATION DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Türkiye EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Pelva Master Kegel Exercise Device by Ves-Vacuum International — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 8964003967Ves-263H5 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ves-Vacuum International
- EUDAMED SRN
- PK-MF-000040378
- Authorised Representative
- KHANG BAO INTERNATIONAL KFT HU-AR-000034102
Sources (1)
- EUDAMED df7bf825-02b9-4336-9601-8988cf96070e 61 fields · synced Jun 18, 2026