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23G shielded wide angle endoillumination probe

EUDAMED

Class IIa (EU MDR)

Ref 192816

by Optikon 2000 S.p.A.

Identity

Trade Name
23G shielded wide angle endoillumination probe EUDAMED
Device Name
25G shielded wide angle endoillumination probe EUDAMED
Model / Reference
192816 EUDAMED

Identifiers

Primary DI / UDI-DI
08059308009736 EUDAMED
Basic UDI-DI
8059308SUR_ENP_005VH EUDAMED
EMDN Code
Q021108 OPHTHALMIC SURGERY PROBES, SINGLE-USE 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 shielded wide angle endoillumination probe by Optikon 2000 S.p.A. — 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
Optikon 2000 S.p.A.
EUDAMED SRN
IT-MF-000017618

Sources (1)

  • EUDAMED 045fd9b1-d7a6-48fe-8438-70ff2162edd0 61 fields · synced Jun 19, 2026