Identity
- Trade Name
- WHO Probe EUDAMED
- Device Name
- WHO Probe EUDAMED
- Model / Reference
- MD3502 EUDAMED
Identifiers
- Primary DI / UDI-DI
- G520MD35020 EUDAMED
- Basic UDI-DI
- ++G520MD3502KW EUDAMED
- EMDN Code
- L159003 DENTAL AND PERIODONTAL PROBES AND EXPLORERS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
WHO Probe by Medspo — 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 | ++G520MD3502KW | Class I | Active |
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Manufacturer
- Manufacturer
- Medspo
- EUDAMED SRN
- PK-MF-000037594
- Authorised Representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Sources (1)
- EUDAMED da716755-6434-477d-85ce-cb0f43ae4ff2 61 fields · synced Jun 17, 2026