Asmb
Country not established
- Devices
- 1
What Asmb makes
Asmb manufactures the ROSEALAE, a medical device designed for sealing and securing vascular access sites, reducing the risk of infection and leakage in clinical settings.
The ROSEALAE is classified as a Class I device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Rosealae Ref K782001
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Asmb have in the registry?
The registry currently lists 1 device for Asmb. Devices recorded under merged duplicate company entries are counted once.
Which registries list Asmb's devices?
Among its 1 most recently registered device, Asmb has devices listed in FDA 510(k) (1 device).
What risk classes do Asmb's devices fall under?
Among its 1 most recently registered device, the classes recorded for Asmb's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Asmb in the registry?
The most recently registered devices listed for Asmb include ROSEALAE.