Botiss mucoderm - HSA Registration DE0508248
Access comprehensive regulatory information for Botiss mucoderm in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0508248 and owned by Biotiss biomaterials GmbH. The device was registered on June 27, 2023.
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.
mucoderm® is indicated for the treatment of oral soft tissue defects and for the regeneration and augmentation of soft tissues around teeth or implants, as well as in edentulous areas. - Treatment of recession defects combined with all the current mucogingival surgical techniques (e.g. coronally and laterally advanced flap, tunnel technique) - Soft tissue augmentation around teeth and implants to widen the keratinized gingiva (Vestibuloplasty) or to thicken the soft tissue - Thickening of the soft tissue alone or in combination with bone grafting in case of bone wall defects, for alveolar ridge augmentation or for prosthetic restoration also in preparation for subsequent augmentative interventions - Covering of extraction sockets for immediate or delayed implantation (e.g. socket seal technique) - Oral wound coverage after tissue transplant harvesting or following tumour surgery