Dms
Country not established
- Devices
- 1
What Dms makes
Dms manufactures a restraining stretcher, designed for patient immobilization and secure transport in medical settings.
The restraining stretcher is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Restraining Stretcher Ref K924275
510(k) 510(k)
Frequently asked questions
How many devices does Dms have in the registry?
The registry currently lists 1 device for Dms. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dms's devices?
Among its 1 most recently registered device, Dms has devices listed in FDA 510(k) (1 device).
What risk classes do Dms's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dms's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dms in the registry?
The most recently registered devices listed for Dms include RESTRAINING STRETCHER.