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Retinal Dual Chandelier 25G for Trocar - Connector S

EUDAMED

Class IIa (EU MDR)

Ref AK-0472/SModel Retinal Chandelier/Candelieri Ref AK-0419/S2

by Aktive Srl

Identity

Trade Name
Retinal Dual Chandelier 25G for Trocar - Connector S EUDAMED
Device Name
Retinal Chandelier/Candelieri EUDAMED
Model / Reference
Retinal Chandelier/Candelieri EUDAMED
AK-0472/S EUDAMED
AK-0419/S2 EUDAMED

Identifiers

Primary DI / UDI-DI
08052276027030 EUDAMED
08052276021267 EUDAMED
Basic UDI-DI
8052276FT0004ID1CV EUDAMED
Unit of Use DI
08056477559444 EUDAMED
08052276016652 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

Retinal Dual Chandelier 25G for Trocar - Connector S 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 (2)

  • EUDAMED 49c9e70a-c590-4a5e-8a8d-a2847898498e 61 fields · synced Aug 2, 2026
  • EUDAMED 9a288f6d-87e1-4aac-a665-d173341be19f 61 fields · synced May 18, 2026