Identity
- Trade Name
- VieSID® Occlusogram Wax EUDAMED
- Model / Reference
- Arti-Wax EUDAMED04-000060 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +E210040000601Q EUDAMED
- Basic UDI-DI
- ++E21011x2x2xArtiWaxZS EUDAMED
- Unit of Use DI
- +E210040000600P EUDAMED
- EMDN Code
- Q01020203 OCCLUSAL WAXES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
VieSID® Occlusogram Wax by Dr. Jean Bausch GmbH & Co. KG — 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 | ++E21011x2x2xArtiWaxZS | Class I | Active |
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Manufacturer
- Manufacturer
- Dr. Jean Bausch GmbH & Co. KG
- EUDAMED SRN
- DE-MF-000005577
Sources (1)
- EUDAMED 543d2190-8e46-4874-9a17-6c6236f5a05e 61 fields · synced Oct 7, 2026