Nucletron B.V.
Active in EUDAMEDNetherlandsfrom SRN EUDAMED FDA SRN NL-MF-000000753 FEI 3002807741
- Devices
- 5
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Fixation Element Ref 153002
Regimes: CE MDR Registry: EUDAMEDLumenCare Azure Ref K262383
Regimes: 510(k) Registry: 510(k)Esophageal Applicator 12 mm Flexitron Ref 154104
Regimes: CE MDR Registry: EUDAMEDFixation Clip Ref 153003
Regimes: CE MDR Registry: EUDAMEDEsophageal Applicator 6 mm Flexitron Ref 154101
Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- NL-MF-000000753
- FDA FEI number
- 3002807741
- EU VAT number
- NL818238240B01
- EUDAMED status
- Active
- EUDAMED registered name
- Nucletron B.V.
- Registered address
- 1, Waardgelder, 3905 TH, Veenendaal, Netherlands
- [email protected]
- PRRC contact
- Rigo Meens
Frequently asked questions
How many devices does Nucletron B.V. have in the registry?
The registry currently lists 5 devices for Nucletron B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nucletron B.V.'s devices?
Among its 5 most recently registered devices, Nucletron B.V. has devices listed in EUDAMED (4 devices) and FDA 510(k) (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Nucletron B.V.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Nucletron B.V.'s devices are Class I, Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nucletron B.V. in the registry?
The most recently registered devices listed for Nucletron B.V. include Fixation Element, LumenCare Azure, Esophageal Applicator 12 mm Flexitron and Fixation Clip.