Medical Monitors Pty., Ltd.
AustraliaFDA applicant, unverified
- Devices
- 2
What Medical Monitors Pty., Ltd. makes
Medical Monitors Pty., Ltd. manufactures the MEMO pulse oximeter, a device used for non-invasive monitoring of blood oxygen saturation (SpO₂) and pulse rate in patients.
The MEMO pulse oximeter is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Bpfone, Model Ua 767IT Ref K010751
Regimes: 510(k) Registry: 510(k)Per, Model Memo Ref K030218
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Monitors Pty., Ltd. have in the registry?
The registry currently lists 2 devices for Medical Monitors Pty., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Monitors Pty., Ltd.'s devices?
Among its 2 most recently registered devices, Medical Monitors Pty., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medical Monitors Pty., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medical Monitors Pty., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Monitors Pty., Ltd. in the registry?
The most recently registered devices listed for Medical Monitors Pty., Ltd. include BPFONE, MODEL UA 767IT and PER, MODEL MEMO.