Simed
Country not established
- Devices
- 1
What Simed makes
SIMED manufactures the S-100 Pulse Oximeter, a device used for non-invasive monitoring of blood oxygen saturation (SpO₂) and pulse rate in patients.
The S-100 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
Simed S-100 Pulse Oximeter Ref K873896
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Simed have in the registry?
The registry currently lists 1 device for Simed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Simed's devices?
Among its 1 most recently registered device, Simed has devices listed in FDA 510(k) (1 device).
What risk classes do Simed's devices fall under?
Among its 1 most recently registered device, the classes recorded for Simed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Simed in the registry?
The most recently registered devices listed for Simed include SIMED S-100 PULSE OXIMETER.