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Knife

EUDAMED

Class I (EU MDR)

Ref DK080Model Knife

by CILITA Ltd.

Identity

Device Name
Knife EUDAMED
Model / Reference
Knife EUDAMED
DK080 EUDAMED

Identifiers

Primary DI / UDI-DI
04610274531542 EUDAMED
Basic UDI-DI
468017344CILKNFBK EUDAMED
EMDN Code
L0102 SURGICAL KNIVES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Knife by CILITA Ltd. — Class I — 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
CILITA Ltd.
EUDAMED SRN
RU-MF-000041168
Authorised Representative
Arazy Group GmbH DE-AR-000007685

Sources (1)

  • EUDAMED 0ef23aa7-c1ca-4f1b-9274-ba1663a5cee0 61 fields · synced Jun 19, 2026