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Cathvision ApS

Denmark DK-MF-000008517 Last updated 22 Oct 2026

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Devices
7
Registries
EUDAMEDGUDIDFDA
FDA recalls
0

Catalogue7

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

Notified body 1912 1 certificate

  • 20M00035SUP01 Supplemented

    Quality management system EU MDR

    Issued
    14 Oct 2026
    Expires
    18 Feb 2030
    Valid from
    15 Oct 2026
    Reason
    Other

Notified bodies

  • Notified body 1912

What Cathvision ApS makes

Cathvision ApS manufactures cables and accessories for electrocardiogram (ECG) monitoring, including the IECG Pin Box, Blood Pressure Cable, ECGenius System, ECG Trunk Cable, and Stimulator Cable. These products are designed to connect ECG devices to monitoring systems, ensuring proper signal transmission and patient data acquisition.

The company’s portfolio includes devices classified as Class I and Class IIb under EU regulations, with all relevant products listed in the eudamed database. Cathvision ApS is based in Denmark.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Cathvision ApS manufacture?

Cathvision ApS specializes in cables and accessories for electrocardiogram (ECG) monitoring. Their products include components like the IECG Pin Box, Blood Pressure Cable, ECGenius System, ECG Trunk Cable, and Stimulator Cable. These devices are designed to facilitate connections between ECG equipment and monitoring systems, ensuring accurate signal transmission and patient data collection.

Where is Cathvision ApS based?

Cathvision ApS is headquartered in Denmark (DK). The company’s location is relevant for understanding its regulatory framework and compliance context, particularly under EU medical device regulations.

Which regulatory registries list Cathvision ApS’s devices?

Cathvision ApS’s devices are listed in the eudamed database, which is the official EU registry for medical devices. Listing in eudamed is required for devices placed on the EU market, ensuring transparency and traceability for regulatory oversight.

How are Cathvision ApS’s devices classified under EU regulations?

Cathvision ApS’s devices fall under Class I and Class IIb classifications under EU medical device regulations. Classification determines the regulatory requirements for conformity assessment, with Class IIb devices typically requiring additional scrutiny due to their higher risk potential compared to Class I.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Denmark
Address
37, Lygten, Copenhagen, Denmark
PRRC contact
Mads Frisenborg Marker
EUDAMED SRN
DK-MF-000008517
FDA FEI number
3017401510
DUNS number
305415202