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Vitrectomy Cutter Sophi 23g

EUDAMED

Class IIa (EU MDR)

Ref 1401-2323Model Vitrectomy Cutter/Vitrectomo

by Aktive Srl

Identity

Trade Name
VITRECTOMY CUTTER SOPHI 23G EUDAMED
Device Name
Vitrectomy Cutter/Vitrectomo EUDAMED
Model / Reference
Vitrectomy Cutter/Vitrectomo EUDAMED
1401-2323 EUDAMED

Identifiers

Primary DI / UDI-DI
08052276013330 EUDAMED
Basic UDI-DI
8052276FT0003HJ EUDAMED
Unit of Use DI
08052276015211 EUDAMED
EMDN Code
Q020499 VITRECTOMY DEVICES - 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

Vitrectomy Cutter Sophi 23g 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 1e4f0c25-1635-4641-8078-5a35e8a95911 61 fields · synced Jun 19, 2026