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Coagulation RF Cable

EUDAMED

Class I (EU MDR)

Ref CSK-2000-3Model CSK-2060Ref A001370-1

by AtriCure, Inc.

Identity

Trade Name
Coagulation RF Cable EUDAMED
Device Name
Coagulation RF Cable EUDAMED
Model / Reference
CSK-2060 EUDAMED
CSK-2000-3 EUDAMED
A001370-1 EUDAMED

Identifiers

Primary DI / UDI-DI
10840143910432 EUDAMED
10840143910418 EUDAMED
Basic UDI-DI
08401439000000000000011ZE EUDAMED
EMDN Code
C020301 ARRHYTHMOGENIC FOCI RADIOFREQUENCY ABLATION CATHETERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Category: Cardiac radio-frequency ablation system catheter

Coagulation RF Cable by Atricure, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac radio-frequency ablation system catheter.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
AtriCure, Inc.
EUDAMED SRN
US-MF-000002974
Authorised Representative
AtriCure Europe B.V. NL-AR-000000165

Sources (2)

  • EUDAMED ce6057b9-3737-400f-b787-b0dce96c709c 61 fields · synced Jul 29, 2026
  • EUDAMED 44e920b7-dad7-41c7-9f06-848e40223372 61 fields · synced May 18, 2026