Cilag GmbH International
Country not established
- Devices
- 3
What Cilag GmbH International makes
Cilag GmbH International manufactures blood glucose monitoring systems, including standalone meters and integrated systems with sync capabilities. These devices measure glucose levels for diabetes management, featuring features like test strip compatibility and connectivity options for data tracking.
The company’s portfolio is regulated under Class II devices in the US, with products authorised via the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Onetouch Verio Blood Glucose Monitoring System Ref K131363
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cilag GmbH International have in the registry?
The registry currently lists 3 devices for Cilag GmbH International. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cilag GmbH International's devices?
Among its 3 most recently registered devices, Cilag GmbH International has devices listed in FDA 510(k) (3 devices).
What risk classes do Cilag GmbH International's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cilag GmbH International's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cilag GmbH International in the registry?
The most recently registered devices listed for Cilag GmbH International include ONETOUCH VERIO SYNC BLOOD GLUCOSE MONITORING SYSTEM, ONETOUCH VERIO BLOOD GLUCOSE MONITORING SYSTEM and ONETOUCH VERIO (TM) IQ BLOOD GLUCOSE MONITORING SYSTEM.