Boehringer Ingelheim Pharmaceuticals, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1219205
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Catapress Tourniguet Ref K852277
Regimes: 510(k) Registry: 510(k)Inhalation Aid Ref K863049
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1219205
- Address
- 900 Ridgebury Rd, Ridgefield, CT, 06877
Frequently asked questions
How many devices does Boehringer Ingelheim Pharmaceuticals, Inc. have in the registry?
The registry currently lists 2 devices for Boehringer Ingelheim Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Boehringer Ingelheim Pharmaceuticals, Inc.'s devices?
Among its 2 most recently registered devices, Boehringer Ingelheim Pharmaceuticals, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Boehringer Ingelheim Pharmaceuticals, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Boehringer Ingelheim Pharmaceuticals, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Boehringer Ingelheim Pharmaceuticals, Inc. in the registry?
The most recently registered devices listed for Boehringer Ingelheim Pharmaceuticals, Inc. include CATAPRESS TOURNIGUET and INHALATION AID.