Infectio Diagnostic (I.D.I.), Inc.
Country not established
- Devices
- 3
What Infectio Diagnostic (I.D.I.), Inc. makes
Infectio Diagnostic (I.D.I.), Inc. manufactures the IDI-MRSA and IDI-MRSA ASSAY, which are Class II medical devices.
These devices are listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
Idi-Mrsa Ref K033415
Regimes: 510(k) Registry: 510(k)Idi-Strep B Assay Ref K022504
Regimes: 510(k) Registry: 510(k)Idi-Mrsa Assay Ref K042357
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Infectio Diagnostic (I.D.I.), Inc. have in the registry?
The registry currently lists 3 devices for Infectio Diagnostic (I.D.I.), Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Infectio Diagnostic (I.D.I.), Inc.'s devices?
Among its 3 most recently registered devices, Infectio Diagnostic (I.D.I.), Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Infectio Diagnostic (I.D.I.), Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Infectio Diagnostic (I.D.I.), Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Infectio Diagnostic (I.D.I.), Inc. in the registry?
The most recently registered devices listed for Infectio Diagnostic (I.D.I.), Inc. include IDI-MRSA, IDI-STREP B ASSAY and IDI-MRSA ASSAY.