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Vitrectomy Dual Cutter 20G - Connector B-A

EUDAMED

Class IIa (EU MDR)

Ref AK-0207/BA2Model Vitrectomy Cutter/Vitrectomo Ref AK-0200/BA2

by Aktive Srl

Identity

Trade Name
Vitrectomy Dual Cutter 20G - Connector B-A EUDAMED
Device Name
Vitrectomy Cutter/Vitrectomo EUDAMED
Model / Reference
Vitrectomy Cutter/Vitrectomo EUDAMED
AK-0207/BA2 EUDAMED
AK-0200/BA2 EUDAMED

Identifiers

Primary DI / UDI-DI
08052276011107 EUDAMED
08052276010360 EUDAMED
Basic UDI-DI
8052276FT0003HJ EUDAMED
Unit of Use DI
08056477556481 EUDAMED
08056477556429 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 Dual Cutter 20G - Connector B-A 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 cde8d0b0-9373-41c3-9439-16c35b180119 61 fields · synced Jul 31, 2026
  • EUDAMED 8b3d60c0-8b9e-4fc1-9140-f1f3cdfc85eb 61 fields · synced May 18, 2026