Singapore HSA registration DE0510119
Botiss cerabone plus
Device classification
- Device Class
- CLASS D
- Medical Speciality Area
- Dental
Registration information
- Registration Number
- DE0510119
- Registration Date
- December 06, 2024
- Retention Due Date
- December 05, 2025
Product description
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
Product Owner
- Short Name
- Biotiss biomaterials GmbH
- Address
- Hauptstr 28, 15806 Zossen, GERMANY
Registrant
- Address
- 73 UBI ROAD 1, OXLEY BIZHUB, #10-61/62, SINGAPORE 408733
Importer
- Address
- 73 UBI ROAD 1, OXLEY BIZHUB, #10-61/62, SINGAPORE 408733
Model information
- Model Name(s)
- cerabone plus cerabone plus cerabone plus cerabone plus
- Model Identifier(s)
- 1810 1811 1820 1821
About this record
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.
Free DatabasePowered by Pure Global AIHSA Official DataCLASS D