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23G valved entry system kit

EUDAMED

Class IIa (EU MDR)

Ref 192223

by Optikon 2000 S.p.A.

Identity

Trade Name
23G valved entry system kit EUDAMED
Device Name
27G valved entry system kit EUDAMED
Model / Reference
192223 EUDAMED

Identifiers

Primary DI / UDI-DI
08059308009477 EUDAMED
Basic UDI-DI
8059308SUR_ACC_013JE EUDAMED
EMDN Code
K01010101 TROCAR STANDARD, SINGLE-USE 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

23G valved entry system kit by Optikon 2000 S.p.A. — 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
Optikon 2000 S.p.A.
EUDAMED SRN
IT-MF-000017618

Sources (1)

  • EUDAMED a02c3d43-1a7f-46be-9dc7-9fd5a3c0d16d 61 fields · synced Jun 19, 2026