Cardia International A/S
Denmark DK-MF-000002223 Last updated 17 Sep 2026
- Devices
- 4
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
CardiAid Electrodes- Pediatric Ref F/BRO/02
Cardiaid Electrodes- Adult Ref F/BRO/02
Blostrupmoen® Ref F/BRO/01
CardiAid® Ref F/BRO/02
About
CardiAid.nl is the official importer, distributor, maintenance and service provider for all CardiAid AEDs in the Benelux! Your emails
What Cardia International A/S makes
Cardia International A/S manufactures defibrillator electrodes for pediatric and adult use, including the CardiAid Electrodes, as well as the BLOSTRUPMOEN® defibrillator system and the CardiAid® defibrillator device.
These products fall under EU Device Class IIb and are listed in the EUDAMED registry. The company is based in Denmark.
Frequently asked questions
What types of medical devices does Cardia International A/S manufacture?
Cardia International A/S manufactures defibrillator electrodes designed for both pediatric and adult patients, such as the CardiAid Electrodes. Additionally, the company produces the BLOSTRUPMOEN® defibrillator system and the CardiAid® defibrillator device. These products are specifically designed for emergency cardiac resuscitation.
Where is Cardia International A/S based?
Cardia International A/S is based in Denmark (DK). The company’s headquarters and manufacturing operations are located there, though it may have distribution or service partners in other regions, such as the Benelux.
Which regulatory registries list Cardia International A/S’s devices?
Cardia International A/S’s devices are listed in the EUDAMED registry, which is the European database for medical devices. This registry is used to track and provide transparency on devices that have undergone the necessary conformity assessment procedures under EU regulations.
How are Cardia International A/S’s devices classified under EU regulations?
Cardia International A/S’s devices, including defibrillator electrodes and defibrillator systems, fall under EU Device Class IIb. This classification is determined based on the risk associated with the device’s intended use and its potential impact on patient safety, requiring a higher level of scrutiny and conformity assessment than lower-risk classes.
Information
- Country
- Denmark
- Address
- 33C, Helligkorsvej , Roskilde, Denmark
- Website
- www.cardiaid.com/
- facebook.com/cardiaidaed
- [email protected]
- Phone
- +31852016178
- PRRC contact
- Nesimi Çiçek
- EUDAMED SRN
- DK-MF-000002223