AlCath Flux Red G eXtra

by VascoMed GmbH EUDAMED

Active European Union

Ref 376379

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number426009092BUDI00001F8 Basic UDI-DI	Date2 Sep 2026Registered	StatusActive
European Union	CE/MDR	Number20374GB450260819	Date19 Aug 2026Issued	StatusActive expires 21 Dec 2030

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Map note: Northern Ireland has no dot of its own.

Certificates

1 certificate · EUDAMED

20374GB450260819 Active Supplemented

Technical documentation EU MDR

Notified body

0482

Issued
19 Aug 2026

Expires
21 Dec 2030

Reason
Change approved

Specification

EUDAMED

Device Name: AlCath
Model / Reference: 376379

Primary DI / UDI-DI: 04251883700495
Basic UDI-DI: 426009092BUDI00001F8
EMDN Code: C020301 Arrhythmogenic foci radiofrequency ablation catheters

Device Class: Class III
Market of Registration: Germany

Manufacturer details

EUDAMED SRN: DE-MF-000005571

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Properties

Sterile

Other properties (12)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No