Murex Biotech, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Murex Biotech, Ltd. makes
Murex Biotech, Ltd. makes diagnostic devices such as WELLCOLEX E.COLI O157:H7, which is used to detect E. coli.
The company's portfolio is regulated as Class I devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Wellcolex E.coli O157:H7 Ref K971663
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Murex Biotech, Ltd. have in the registry?
The registry currently lists 1 device for Murex Biotech, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Murex Biotech, Ltd.'s devices?
Among its 1 most recently registered device, Murex Biotech, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Murex Biotech, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Murex Biotech, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Murex Biotech, Ltd. in the registry?
The most recently registered devices listed for Murex Biotech, Ltd. include WELLCOLEX E.COLI O157:H7.