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23G Twedge high speed dual blade vitrectomy probe

EUDAMED

Class IIb (EU MDR)

Ref 192313

by Optikon 2000 S.p.A.

Identity

Trade Name
23G Twedge high speed dual blade vitrectomy probe EUDAMED
Device Name
27G Twedge high speed dual blade vitrectomy probe EUDAMED
Model / Reference
192313 EUDAMED

Identifiers

Primary DI / UDI-DI
08059308009521 EUDAMED
Basic UDI-DI
8059308SUR_ACC_030JE EUDAMED
EMDN Code
Q020499 VITRECTOMY DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIb 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 Twedge high speed dual blade vitrectomy probe by Optikon 2000 S.p.A. — Class IIb — 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 90739494-9c02-4ab6-9429-44d5aa590a94 61 fields · synced Jul 9, 2026