Bioplastics
Country not established
- Devices
- 1
What Bioplastics makes
Bioplastics manufactures the BIOTHANE Patient Restraint, a device designed for securing patients in medical settings to prevent falls or wandering.
The BIOTHANE Patient Restraint is classified as a Class I medical device in the US and is listed under FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Biothane Patient Restraint Ref K991591
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioplastics have in the registry?
The registry currently lists 1 device for Bioplastics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioplastics's devices?
Among its 1 most recently registered device, Bioplastics has devices listed in FDA 510(k) (1 device).
What risk classes do Bioplastics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bioplastics's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Bioplastics in the registry?
The most recently registered devices listed for Bioplastics include BIOTHANE PATIENT RESTRAINT.