Biomedical International Corp.
Country not established
- Devices
- 1
What Biomedical International Corp. makes
Biomedical International Corp. manufactures a bone marrow collection system designed for the extraction and processing of hematopoietic stem cells, primarily used in transplant procedures.
The company’s product portfolio is regulated under FDA’s Class I device classification, with the bone marrow collection system authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Bone & Marrow Cllection System Ref K971268
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomedical International Corp. have in the registry?
The registry currently lists 1 device for Biomedical International Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomedical International Corp.'s devices?
Among its 1 most recently registered device, Biomedical International Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Biomedical International Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biomedical International Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Biomedical International Corp. in the registry?
The most recently registered devices listed for Biomedical International Corp. include BONE & MARROW CLLECTION SYSTEM.