Identity
- Trade Name
- Probe EUDAMED
- Device Name
- Ring Curette-Teardrop EUDAMED
- Model / Reference
- 0402-430 EUDAMED0302-180 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04262463852145 EUDAMED
- Basic UDI-DI
- 426246385PG049M EUDAMED
- Direct Marketing DI
- 04262463852145 EUDAMED
- EMDN Code
- L091201 ORTHOPAEDIC SURGERY RASPS, 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
Probe by Meditec Source 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 | 426246385PG049M | Class I | Active |
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Manufacturer
- Manufacturer
- Meditec Source GmbH & Co. KG
- EUDAMED SRN
- DE-MF-000006490
Sources (1)
- EUDAMED a2ecc340-d1fd-47c6-b50b-fd21b946563d 61 fields · synced Jul 12, 2026