Shire Biologics, Inc.
Country not established
- Devices
- 1
What Shire Biologics, Inc. makes
Shire Biologics, Inc. manufactures the Cistem Fluid Transfer Device, available in models 7S2012 and 7S2013. This device is designed for transferring fluids in medical settings, ensuring controlled and sterile handling of biological samples or solutions.
The Cistem Fluid Transfer Device is classified as a Class II medical device under FDA regulations and is recorded in the FDA’s 510(k) clearance database. The company is headquartered in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shire Biologics, Inc. have in the registry?
The registry currently lists 1 device for Shire Biologics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shire Biologics, Inc.'s devices?
Among its 1 most recently registered device, Shire Biologics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Shire Biologics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Shire Biologics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shire Biologics, Inc. in the registry?
The most recently registered devices listed for Shire Biologics, Inc. include CISTEM FLUID TRANSFER DEVICE, MODEL 7S2012 AND 7S2013.