Annidis Health Systems Corp.
CanadaFDA applicant, unverified
- Devices
- 2
What Annidis Health Systems Corp. makes
Annidis Health Systems Corp. manufactures the RHA2020, a reusable hemodialysis machine designed for use in clinical settings to filter blood in patients with kidney failure.
The company’s portfolio is regulated under Class II devices in the US and includes products listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
RHA2020 Ref K111531
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 243651440
- [email protected]
- Phone
- 613 596 1800
Frequently asked questions
How many devices does Annidis Health Systems Corp. have in the registry?
The registry currently lists 2 devices for Annidis Health Systems Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Annidis Health Systems Corp.'s devices?
Among its 2 most recently registered devices, Annidis Health Systems Corp. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Annidis Health Systems Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Annidis Health Systems Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Annidis Health Systems Corp. in the registry?
The most recently registered devices listed for Annidis Health Systems Corp. include RHA RHA2020/2020-U and RHA2020.