Par Medex, Ltd.
Country not established
- Devices
- 1
What Par Medex, Ltd. makes
Par Medex, Ltd. manufactures the MEDAID Dual Channel TENS device, a transcutaneous electrical nerve stimulation (TENS) unit designed for pain management through low-voltage electrical impulses.
The MEDAID Dual Channel TENS is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Medaid Dual Channel Tens Ref K834334
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Par Medex, Ltd. have in the registry?
The registry currently lists 1 device for Par Medex, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Par Medex, Ltd.'s devices?
Among its 1 most recently registered device, Par Medex, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Par Medex, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Par Medex, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Par Medex, Ltd. in the registry?
The most recently registered devices listed for Par Medex, Ltd. include MEDAID DUAL CHANNEL TENS.