Botiss cerabone plus - HSA Registration DE0510119
Access comprehensive regulatory information for Botiss cerabone plus in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0510119 and owned by Biotiss biomaterials GmbH. The device was registered on December 06, 2024.
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.
Cerabone plus is intended for the permanent filling or reconstruction of aseptic bone defects and for volume augmentation in autologous spongiosa transplantation in dental, oral and maxillofacial surgery. Indications: Alveolar ridge augmentation/reconstruction, Filling of bone defects (including after root resection, apicoectomy or cystectomy), Filling of extraction sockets to support alveolar ridge preservation, Sinus floor elevation, Filling of periodontal bone defects, Filling of extraction sockets as part of immediate implantations, Filling of peri-implant bone defects