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Lambert-Kay Titanium Occlusion Clamp 19c

EUDAMED

Class I (EU MDR)

Ref CS5-2040-22

by Cardio Surgical Ltd.

Identity

Device Name
LAMBERT-KAY TITANIUM OCCLUSION CLAMP 19C EUDAMED
Model / Reference
CS5-2040-22 EUDAMED

Identifiers

Primary DI / UDI-DI
05391551752063 EUDAMED
Basic UDI-DI
539155175CS5-2040-22X4 EUDAMED
EMDN Code
L080599 THORACIC SURGERY CLAMPS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

Lambert-Kay Titanium Occlusion Clamp 19c by Cardio Surgical 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

EUDAMED SRN
IE-MF-000011150

Sources (1)

  • EUDAMED ae0466ed-f41d-4798-8fb2-eee0ba5f80d4 61 fields · synced Jun 19, 2026