Cathvision ApS
Denmark DK-MF-000008517 Last updated 22 Oct 2026
Is this your brand? Sign in to claim this brand
- Devices
- 7
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
ECGenius System CVT-0069 R3.0 Ref CVT-0069 R3.0
ECGenius System CVT-0069 R2.0 Ref CVT-0069 R2.0
IECG Pin Box Ref CVHW-0073 R3.0 IECG Pin Box
Blood Pressure Cable Ref CVHW-0015 R2.0 Blood Pressure Cable
ECGenius System Ref CVT-0069 R3.2 ECGenius System
ECG Trunk Cable Ref CVHW-0072 R2.0 ECG Trunk Cable
Stimulator Cable Ref CVHW-0016 R1.0 Stimulator Cable
EUDAMED certificates
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
Related companies
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.
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.
Information
- Country
- Denmark
- Address
- 37, Lygten, Copenhagen, Denmark
- Website
- www.cathvision.com
- [email protected]
- PRRC contact
- Mads Frisenborg Marker
- EUDAMED SRN
- DK-MF-000008517
- FDA FEI number
- 3017401510
- DUNS number
- 305415202