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20G Laser Probe, straight

EUDAMED

Class IIa (EU MDR)

Ref AK-0430/SMHModel Fibre laser/ Laser Fiber

by Aktive Srl

Identity

Trade Name
20G Laser Probe, straight EUDAMED
Device Name
Fibre laser/ Laser Fiber EUDAMED
Model / Reference
Fibre laser/ Laser Fiber EUDAMED
AK-0430/SMH EUDAMED

Identifiers

Primary DI / UDI-DI
08052276023360 EUDAMED
Basic UDI-DI
8052276FT0004ID4D3 EUDAMED
Unit of Use DI
08056477559093 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

20G Laser Probe, straight 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

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Manufacturer

Manufacturer
Aktive Srl
EUDAMED SRN
IT-MF-000007813

Sources (1)

  • EUDAMED c5a6d6ae-704d-4a8d-922b-e73362513285 61 fields · synced May 21, 2026