Identity
- Trade Name
- EMBOTRAP II EUDAMED
- Model / Reference
- ET-007-533 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-IEMF00000761200000156 EUDAMED
- Basic UDI-DI
- B-IEMF00000761200000156 EUDAMED
- EMDN Code
- C019010 INTRAVASCULAR RECANALISATION SYSTEMS EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Ireland 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
Embotrap Ii by Neuravi Limited — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-IEMF00000761200000156 | Class III | Active |
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Manufacturer
- Manufacturer
- Neuravi Limited
- EUDAMED SRN
- IE-MF-000007612
Sources (1)
- EUDAMED 3f7c53a7-d0b4-419a-8147-eb0f9dfa3bf8 61 fields · synced Jul 13, 2026