Identity
- Trade Name
- Wellion PRO2 LANCING DEVICE EUDAMED
- Device Name
- Wellion PRO2 LANCING DEVICE EUDAMED
- Model / Reference
- WELL920 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 09010727017091 EUDAMED
- Basic UDI-DI
- 90107270007L2 EUDAMED
- Direct Marketing DI
- 09010727017091 EUDAMED
- EMDN Code
- V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER 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
Wellion PRO2 LANCING DEVICE by MED TRUST Handelsges.m.b.H. — 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 | 90107270007L2 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- MED TRUST Handelsges.m.b.H.
- EUDAMED SRN
- AT-MF-000000311
Sources (1)
- EUDAMED 3b9a08af-8077-4ff1-9c32-c6785c40a7e6 61 fields · synced Jul 29, 2026