Huinno Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Huinno Co., Ltd. makes
Huinno Co., Ltd. manufactures the MEMO Patch M (MPT-E08R-UNC01), a medical device designed for continuous monitoring of physiological parameters such as heart rate and respiratory rate. This patch is intended for use in clinical and ambulatory settings to provide real-time data transmission for patient assessment.
The MEMO Patch M is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
MEMO Patch M (MPT-E08R-UNC01) Ref K243438
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Huinno Co., Ltd. have in the registry?
The registry currently lists 1 device for Huinno Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Huinno Co., Ltd.'s devices?
Among its 1 most recently registered device, Huinno Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Huinno Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Huinno Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Huinno Co., Ltd. in the registry?
The most recently registered devices listed for Huinno Co., Ltd. include MEMO Patch M (MPT-E08R-UNC01).