Biosystems
Country not established
- Devices
- 5
What Biosystems makes
Biosystems manufactures containment systems for biological safety, including the BIOBOX TRAPTOP and BIOBOX WITH FUNNEL TOP in sizes small, medium, large, and extra-large. The company also produces laboratory sharps barrels designed for safe disposal of contaminated sharps. These products are intended for use in controlled environments to reduce exposure risks.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States, where Biosystems is based.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Cancel Ref K812582
Regimes: 510(k) Registry: 510(k)Laboratory Sharps Barrel Ref K950899
Regimes: 510(k) Registry: 510(k)Cuprident Ref K851073
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biosystems have in the registry?
The registry currently lists 5 devices for Biosystems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biosystems's devices?
Among its 5 most recently registered devices, Biosystems has devices listed in FDA 510(k) (5 devices).
What risk classes do Biosystems's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Biosystems's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biosystems in the registry?
The most recently registered devices listed for Biosystems include BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE), CANCEL, LABORATORY SHARPS BARREL and CUPRIDENT.