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Octax NaviLase upgrade
EUDAMEDClass IIa (EU MDR)
Ref 19310/0147Model Octax NaviLase upgrade
Identity
- Trade Name
- Octax NaviLase upgrade EUDAMED
- Device Name
- Octax NaviLase upgrade EUDAMED
- Model / Reference
- Octax NaviLase upgrade EUDAMED19310/0147 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04260604170042 EUDAMED
- Basic UDI-DI
- 4260604170045N EUDAMED
- EMDN Code
- Z12080205 OOCYTE LASER DRILLS EUDAMED
Classification
- Device Class
- Class IIa 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
Octax NaviLase upgrade by Vitrolife GmbH — Class IIa — 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 | 4260604170045N | Class IIa | Active |
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Manufacturer
- Manufacturer
- Vitrolife GmbH
- EUDAMED SRN
- DE-MF-000007378
Sources (1)
- EUDAMED ccb1cf7e-0cc9-41c0-8f36-07e7030268b3 61 fields · synced Jun 19, 2026