Hersill, S.L.
SpainFDA applicant, unverified FDA FEI 3007360714
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Hersill, S.L. makes
Hersill, S.L. manufactures portable suction units and revivators, which are medical devices used for suction and resuscitation purposes.
The company's products are classified as Class II medical devices and are listed in the FDA 510(k) registry. Hersill, S.L. is based in the US.
Catalogue
V7 Portable Suction Units Ref K093241
Regimes: 510(k) Registry: 510(k)Revivator Ref K094003
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3007360714
- Address
- C/ PUERTO DE NAVACERRADA, 3, MOSTOLES (MADRID) Madrid(Province)
Frequently asked questions
How many devices does Hersill, S.L. have in the registry?
The registry currently lists 2 devices for Hersill, S.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hersill, S.L.'s devices?
Among its 2 most recently registered devices, Hersill, S.L. has devices listed in FDA 510(k) (2 devices).
What risk classes do Hersill, S.L.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hersill, S.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hersill, S.L. in the registry?
The most recently registered devices listed for Hersill, S.L. include V7 PORTABLE SUCTION UNITS and REVIVATOR.