Fluidda NV
Inactive in EUDAMED since 2025Belgiumfrom SRN EUDAMED FDA SRN BE-MF-000006480 FEI 3011786147
Part of Fluidda, Inc.
Inactive. This company's EUDAMED actor record is marked inactive. Check the current status before ordering.
- Devices
- 1
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
0 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
Catalogue
Broncholab Ref 1.1.1
CE MDR, withdrawn EUDAMED
Company details
- EUDAMED SRN
- BE-MF-000006480
- FDA FEI number
- 3011786147
- EU VAT number
- BE0877 160 706
- EUDAMED status
- Inactive since 2025
- EUDAMED registered name
- FLUIDDA NV
- Registered address
- Groeningenlei 132, 2550, Antwerp, Belgium
- Website
- www.fluidda.com/
- [email protected]
- Phone
- +32/(0)3 450 87 20
- PRRC contact
- Rita João
EUDAMED certificates
1 certificate0 valid, 0 expired, 1 withdrawn or suspendedMDR 1
Notified body 1912 1 certificate
- 20M00107CRT01 Cancelled
Quality management system EU MDR
- Issued
- 21 Jun 2022
- Expires
- 21 Jun 2025
- Reason
- Other
Frequently asked questions
How many devices does FLUIDDA NV have in the registry?
The registry currently lists 1 device for FLUIDDA NV. Devices recorded under merged duplicate company entries are counted once.
Which registries list FLUIDDA NV's devices?
Among its 1 most recently registered device, FLUIDDA NV has devices listed in EUDAMED (1 device).
What risk classes do FLUIDDA NV's devices fall under?
Among its 1 most recently registered device, the classes recorded for FLUIDDA NV's devices are Class IIa. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for FLUIDDA NV?
EUDAMED lists 1 certificate for FLUIDDA NV (quality management system) under MDR. The most recent was issued on 2022-06-21.
What are the newest devices from FLUIDDA NV in the registry?
The most recently registered devices listed for FLUIDDA NV include Broncholab.