← Back to catalogue

Retinal Chandelier 23G with Trocar - Connector E

EUDAMED

Class IIa (EU MDR)

Ref AK-0418/EModel Retinal Chandelier/Candelieri

by Aktive Srl

Identity

Trade Name
Retinal Chandelier 23G with Trocar - Connector E EUDAMED
Device Name
Retinal Chandelier/Candelieri EUDAMED
Model / Reference
Retinal Chandelier/Candelieri EUDAMED
AK-0418/E EUDAMED

Identifiers

Primary DI / UDI-DI
08052276020970 EUDAMED
Basic UDI-DI
8052276FT0004ID1CV EUDAMED
Unit of Use DI
08052276003331 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 Chandelier 23G with Trocar - Connector E 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Aktive Srl
EUDAMED SRN
IT-MF-000007813

Sources (1)

  • EUDAMED 7e1b72a8-3021-4b0d-99c2-36b8efe3ae90 61 fields · synced Jul 9, 2026