Becton Dickinson, S.A.
Active in EUDAMEDSpainfrom SRN EUDAMED FDA SRN ES-MF-000016479 FEI 3002682307
- Devices
- 129
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
What Becton Dickinson, S.A. makes
Becton Dickinson, S.A. manufactures the Emerald device.
The Emerald device is classified as Class IIa and is listed in the EUDAMED registry. The company is based in Spain.
Catalogue
Search and filter all 129 devicesShowing 1-50 of 129
Company details
- EUDAMED SRN
- ES-MF-000016479
- FDA FEI number
- 3002682307
- EU VAT number
- ESA50140706
- EUDAMED status
- Active
- EUDAMED registered name
- Becton Dickinson, S.A.
- Registered address
- s/n, Camino de Valdeoliva, 28750, San Agustin del Guadalix, Spain
- [email protected]
- PRRC contact
- Elena Morollon
Frequently asked questions
How many devices does Becton Dickinson, S.A. have in the registry?
The registry currently lists 129 devices for Becton Dickinson, S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Becton Dickinson, S.A.'s devices?
Among its 50 most recently registered devices, Becton Dickinson, S.A. has devices listed in EUDAMED (50 devices).
What risk classes do Becton Dickinson, S.A.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Becton Dickinson, S.A.'s devices are Class I and Class IIa. Each device page shows its own class and authorisation.
What are the newest devices from Becton Dickinson, S.A. in the registry?
The most recently registered devices listed for Becton Dickinson, S.A. include Emerald, SOLOSHOT, Plastipak and DISCARDIT.