Identity
- Device Name
- Pusher rod EUDAMED
- Model / Reference
- UNT-I-2075 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04260706010697 EUDAMED
- Basic UDI-DI
- 42607060101guideBG EUDAMED
- Direct Marketing DI
- 04260706010697 EUDAMED
- EMDN Code
- L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
Pusher rod by Unintech GmbH — 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 | 42607060101guideBG | Class I | Active |
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Manufacturer
- Manufacturer
- Unintech GmbH
- EUDAMED SRN
- DE-MF-000005136
Sources (1)
- EUDAMED 8da6e9c8-a8b9-4b81-a933-e9b4fefe5a8f 61 fields · synced Jul 23, 2026