Inmedix, Inc.
United Statesfrom the FDA registration address FDA FEI 3036039911
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Inmedix, Inc. makes
Inmedix, Inc. manufactures professional multichannel electrocardiograph systems designed for clinical use, including the CloudHRV™ System and its variant (100-01-001). These devices record and analyze heart rhythms with multiple leads for diagnostic purposes.
The company’s products are classified as Class II devices under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
CloudHRV™ System (100-01-001) Ref K241217
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3036039911
- DUNS number
- 117788373
- Address
- 17837 First Avenue South, #6, Normandy Park, WA, 98148
Frequently asked questions
How many devices does Inmedix, Inc. have in the registry?
The registry currently lists 3 devices for Inmedix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inmedix, Inc.'s devices?
Among its 3 most recently registered devices, Inmedix, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Inmedix, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Inmedix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inmedix, Inc. in the registry?
The most recently registered devices listed for Inmedix, Inc. include CloudHRV™ System 10001001, CloudHRV™ System 68481 and CloudHRV™ System (100-01-001).