Fysicon B.V.
Netherlands NL-MF-000002694 Last updated 25 Oct 2026
- Devices
- 92
- Registries
- EUDAMEDGUDID
- FDA recalls
- 0
Catalogue
SUB-D Female to BNC cable 25 m Ref 01323050
DataLinQ RDM Cloud Ref 01075066
10 Lead (AHA) radiopaque lead wire set with grabber Ref 01567033
QMAPP AUX to BNC cable Ref 01076504
QMAPP 10 Lead ECG trunk cable, IEC 165 cm Ref 01567031
QMAPP System Cable White (1000cm) Ref 01077007
Silicon soft cover SpO2 sensor Adult (Reusable) Ref 01567053
Qmapp Hemo Ref 01076101
QMAPP 5 Lead ECG Trunk cable, AHA 320 CM Ref 01567057
QMAPP IBP Connection cable B.Braun (300 cm) Ref 01802004
QMAPP NIBP Connection hose 365 CM Ref 01567082
IBP Cable Medex Logical – David/Metek (320CM) Ref 01802045
QMAPP IBP Connection cable BD, Argon 320 CM Ref 01567022
IBP Cable Medex Logical – Siemens 7p (320CM) Ref 01802043
Qmapp Hemo Lt Ref 01076103
IBP Cable Medex Logical – Prucka (320CM) Ref 01802046
QMAPP IBP Connection cable - PVB, Codan 320 cm Ref 01802014
Evocs Ref 010147xxx
QMAPP IBP Connection cable - Medex Logcal 320 CM Ref 01802034
NiBP Adapter, Dual lumen cuff to Single hose Ref 01567094
QMAPP 10 Lead ECG Trunk cable, AHA, 320 CM Ref 01567096
Reusable NiBP Cuff, Infant (Orange), 8-13 cm Ref 01853001
QMAPP Cardiac Output Y-connection cable Ref 01802053
Showing 51-92 of 92
EUDAMED certificates
Notified body 1912 3 certificates
- 24M00192CRT01 Reissued
Quality management system EU MDR
- Issued
- 14 Mar 2025
- Expires
- 14 Mar 2030
- 24M00192SUP01 Supplemented
Quality management system EU MDR
- Issued
- 23 Apr 2026
- Expires
- 14 Mar 2030
- Reason
- Other
- 21M00066CRT02 Expired
Quality management system EU MDR
- Issued
- 17 Oct 2024
- Expires
- 14 Mar 2025
- Reason
- Other
Related companies
Notified bodies
- Notified body 1912
About
Fysicon focuses on the development of both innovative hardware and advanced medical applications for hospitals and research institutions.
What Fysicon B.V. makes
Fysicon B.V. manufactures medical cables and lead wire sets for electrocardiogram (ECG) monitoring, including radiopaque and radiolucent variants with snap connectors and grabber attachments. Their portfolio also includes invasive blood pressure (IBP) connection cables for various medical devices, such as those from Abbott, Memscap/SensoNor, and Angiodynamics, as well as reusable non-invasive blood pressure (NiBP) cuffs for adult patients. Additional products include ECG trunk cables and specialized connection cables for physiological monitoring systems.
The company’s devices fall under EU medical device classifications of Class I and Class IIb, reflecting varying levels of risk and regulatory oversight. These products are listed in the EU’s eudamed registry, ensuring traceability and compliance with European Union medical device regulations. Fysicon B.V. is based in the Netherlands.
Frequently asked questions
What types of medical devices does Fysicon B.V. manufacture?
Fysicon B.V. specializes in cables and lead wire sets primarily used for ECG monitoring, including both radiopaque and radiolucent variants. Their products also cover invasive blood pressure (IBP) connection cables for various medical devices, such as those from Abbott, Memscap/SensoNor, and Angiodynamics, as well as reusable non-invasive blood pressure (NiBP) cuffs for adult patients. These devices support physiological monitoring in hospitals and research settings.
Where is Fysicon B.V. based, and what does this mean for its regulatory compliance?
Fysicon B.V. is based in the Netherlands, which means its devices are subject to EU medical device regulations. Since the company’s products are listed in the EU’s eudamed registry, they comply with traceability requirements under EU Medical Device Regulation (MDR) or In Vitro Diagnostic Regulation (IVDR). Listing in eudamed ensures transparency and aligns with EU-wide regulatory standards.
How are Fysicon B.V.’s devices classified under EU regulations, and why does this matter?
Fysicon B.V.’s devices fall under Class I and Class IIb classifications under EU medical device rules. Class I devices pose the lowest risk and typically require general safety and performance requirements, while Class IIb devices involve higher risks (e.g., invasive monitoring cables) and require additional scrutiny, such as clinical evaluations or specialized testing. This classification determines the regulatory scrutiny and documentation needed for compliance.
Are Fysicon B.V.’s devices listed in any official regulatory registries, and what does this indicate?
Yes, Fysicon B.V.’s devices are listed in the eudamed registry, the EU’s official database for medical devices. This listing confirms that the manufacturer has registered its products with the relevant national competent authorities, fulfilling traceability and transparency requirements under EU medical device laws. It does not imply approval but ensures compliance with EU regulatory frameworks.
What kinds of connectors and specialized features do Fysicon B.V.’s lead wire sets and cables include?
Fysicon B.V.’s lead wire sets and cables include snap connectors for easy attachment, grabber attachments for secure handling, and radiopaque/radiolucent variants to ensure visibility during imaging procedures. Their ECG trunk cables and IBP connection cables are designed for compatibility with specific medical devices (e.g., Abbott, Angiodynamics), ensuring seamless integration into monitoring systems while maintaining safety and functionality.
Information
- Country
- Netherlands
- Address
- 114, Hoogheuvelstraat , Oss, Netherlands
- Website
- www.fysicon.com
- nl.linkedin.com/company/fysicon
- facebook.com/FysiconNL
- [email protected]
- Phone
- +31 412 65 33 33
- PRRC contact
- Patricia Steenstra
- EUDAMED SRN
- NL-MF-000002694
- DUNS number
- 404866654