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23G Laser Probe, curved
EUDAMEDClass IIa (EU MDR)
Ref AK-0435/SMHModel Fibre laser/ Laser Fiber
by Aktive Srl
Identity
- Trade Name
- 23G Laser Probe, curved EUDAMED
- Device Name
- Fibre laser/ Laser Fiber EUDAMED
- Model / Reference
- Fibre laser/ Laser Fiber EUDAMEDAK-0435/SMH EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08052276025524 EUDAMED
- Basic UDI-DI
- 8052276FT0004ID4D3 EUDAMED
- Unit of Use DI
- 08056477559147 EUDAMED
- EMDN Code
- Q021199 OPHTHALMIC SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Italy 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
23G Laser Probe, curved by Aktive Srl — 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 | 8052276FT0004ID4D3 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Aktive Srl
- EUDAMED SRN
- IT-MF-000007813
Sources (1)
- EUDAMED 9178d083-1454-42db-8560-392eaf10de29 61 fields · synced Jul 10, 2026