Organization name

AtriCure, Inc.

SRN

US-MF-000002974

Manufacturer status

Active

Primary placement in Netherlands; available across 30 countries total.

Trade name

Coagulation RF Cable

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

10840143910432

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

08401439000000000000011ZE

Reference / catalog number

CSK-2000-3

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

EPi-Sense Guided Coagulation System with VisiTrax Coagulation RF Cable

Additional information URL

https://www.atricure.com/

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• C020301ARRHYTHMOGENIC FOCI RADIOFREQUENCY ABLATION CATHETERS

• Class I medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.