Celltech Diagnostics, Ltd.
Country not established
- Devices
- 1
What Celltech Diagnostics, Ltd. makes
Celltech Diagnostics, Ltd. manufactures the CELLABS GIARDIA CEL I.F. TEST, an immunofluorescent assay for detecting *Giardia lamblia* antigens in stool samples, used for diagnosing gastrointestinal infections.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Cellabs Giardia Cel I.F. Test Ref K912152
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Celltech Diagnostics, Ltd. have in the registry?
The registry currently lists 1 device for Celltech Diagnostics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Celltech Diagnostics, Ltd.'s devices?
Among its 1 most recently registered device, Celltech Diagnostics, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Celltech Diagnostics, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Celltech Diagnostics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Celltech Diagnostics, Ltd. in the registry?
The most recently registered devices listed for Celltech Diagnostics, Ltd. include CELLABS GIARDIA CEL I.F. TEST.