Dr. K.G. Rude
Country not established
- Devices
- 1
What Dr. K.G. Rude makes
Dr. K.G. Rude manufactures the CERVI-TRAC, a device designed for monitoring cervical dilation during childbirth.
The CERVI-TRAC is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Cervi-Trac Ref K791808
510(k) 510(k)
Frequently asked questions
How many devices does Dr. K.G. Rude have in the registry?
The registry currently lists 1 device for Dr. K.G. Rude. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. K.G. Rude's devices?
Among its 1 most recently registered device, Dr. K.G. Rude has devices listed in FDA 510(k) (1 device).
What risk classes do Dr. K.G. Rude's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dr. K.G. Rude's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dr. K.G. Rude in the registry?
The most recently registered devices listed for Dr. K.G. Rude include CERVI-TRAC.