Angiotech Medical Device Technologies
Country not established
- Devices
- 2
What Angiotech Medical Device Technologies makes
Angiotech Medical Device Technologies produces surgical sealants and hemostats designed to control bleeding and promote wound closure during procedures. Their premixed COSEAL Surgical Sealant is formulated for topical application to tissues, while the COSTASIS and DYNASTAT Surgical Hemostats are intended to rapidly stop bleeding in surgical settings.
These devices are classified as Class III under FDA regulations and require Premarket Approval (PMA) authorization. The company’s products are listed in the FDA’s PMA registry, and the manufacturer is based in the United States.
Catalogue
Coseal Surgical Sealant (Premixed) Ref P010022
Regimes: PMA, withdrawn Registry: PMACostasis/Dynastat Surgical Hemostats Ref P990030
Regimes: PMA, withdrawn Registry: PMA
Frequently asked questions
How many devices does Angiotech Medical Device Technologies have in the registry?
The registry currently lists 2 devices for Angiotech Medical Device Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angiotech Medical Device Technologies's devices?
Among its 2 most recently registered devices, Angiotech Medical Device Technologies has devices listed in FDA PMA (2 devices).
What risk classes do Angiotech Medical Device Technologies's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Angiotech Medical Device Technologies's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Angiotech Medical Device Technologies in the registry?
The most recently registered devices listed for Angiotech Medical Device Technologies include COSEAL SURGICAL SEALANT (PREMIXED) and COSTASIS/DYNASTAT SURGICAL HEMOSTATS.