Identity
- Trade Name
- Occlutech Occlusions Pusher EUDAMED
- Device Name
- Occlutech Occlusions Pusher EUDAMED
- Model / Reference
- 50OP120 EUDAMED50OP020 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04260182521878 EUDAMED04260182521861 EUDAMED
- Basic UDI-DI
- 426018252OOPFL EUDAMED
- EMDN Code
- P0780 VASCULAR AND CARDIAC PROSTHESES - ACCESSORIES EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
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
Occlutech Occlusions Pusher by Occlutech GmbH — Class III — 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 | 426018252OOPFL | Class III | Active |
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Manufacturer
- Manufacturer
- Occlutech GmbH
- EUDAMED SRN
- DE-MF-000005104
Sources (2)
- EUDAMED 5ff5ba41-5e23-4d98-8249-51977cfaa6e3 61 fields · synced Jul 26, 2026
- EUDAMED 8768941a-1b35-450a-af7f-165314870005 61 fields · synced May 17, 2026