Microtest
Country not established
- Devices
- 4
What Microtest makes
Microtest manufactures microbiological media and transport systems for clinical specimen collection, including the Modified Micro Test Multi Microbe Medium (M5), Microtest Multi Microbe Medium, and specialized kits like Virapure, Chlamypure, and Mycopure. The company also produces the M4-RT transport medium, a modified version of the M4 formulation designed for preserving microbial samples during transport.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearances. Microtest operates from the United States, with its devices listed in the FDA’s 510(k) registry.
Catalogue
Modified Micro Test Multi Microbe Medium (M5) Ref K941579
Regimes: 510(k) Registry: 510(k)Microtest Multi Microbe Medium Ref K910526
Regimes: 510(k) Registry: 510(k)Virapure, Chlamypure And Mycopure Ref K914894
Regimes: 510(k) Registry: 510(k)M4-Rt Transport Medium, (M4 Modification) Ref K921472
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microtest have in the registry?
The registry currently lists 4 devices for Microtest. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microtest's devices?
Among its 4 most recently registered devices, Microtest has devices listed in FDA 510(k) (4 devices).
What risk classes do Microtest's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Microtest's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Microtest in the registry?
The most recently registered devices listed for Microtest include MODIFIED MICRO TEST MULTI MICROBE MEDIUM (M5), MICROTEST MULTI MICROBE MEDIUM, VIRAPURE, CHLAMYPURE AND MYCOPURE and M4-RT TRANSPORT MEDIUM, (M4 MODIFICATION).