Botiss Jason® Membrane - HSA Registration DE0507431
Access comprehensive regulatory information for Botiss Jason® Membrane in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0507431 and owned by Biotiss biomaterials GmbH. The device was registered on October 31, 2022.
This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
Jason® membrane alone or in combination with suitable augmentation materials (like autogenous bone or other bone substitute materials) is indicated for guided bone and tissue regeneration with simultaneous or later implantation: for sinus floor augmentation and covering / support of the Schneiderian membrane; for alveolar ridge augmentation / reconstruction; for treatment of surgical bone defects, bone wall defects, defects around bone grafts and dental implants; for treatment of periodontal bone defects (one to three-wall defects, class I and II furcation defects); for filling of extraction sockets for immediate or delayed implantation (socket preservation).