Singapore HSA registration DE0507405
botiss cerabone® Granulate
Device classification
- Device Class
- CLASS D
- Medical Speciality Area
- Dental
Registration information
- Registration Number
- DE0507405
- Registration Date
- October 26, 2022
- Retention Due Date
- October 25, 2025
Product description
cerabone® Granulate 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.
Product Owner
- Short Name
- botiss biomaterials GmbH
- Address
- Hauptstr. 28, 15806 Zossen, GERMANY
Registrant
- Address
- 250 NORTH BRIDGE ROAD, RAFFLES CITY TOWER, #19-05, SINGAPORE 179101
Importer
- Address
- 250 NORTH BRIDGE ROAD, RAFFLES CITY TOWER, #19-05, SINGAPORE 179101
Model information
- Model Name(s)
- cerabone® Granulate cerabone® Granulate cerabone® Granulate cerabone® Granulate cerabone® Granulate cerabone® Granulate cerabone® Granulate cerabone® Granulate
- Model Identifier(s)
- BO-1510 BO-1511 BO-1512 BO-1515 BO-1520 BO-1521 BO-1522 BO-1525
About this record
Access comprehensive regulatory information for botiss cerabone® Granulate in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0507405 and owned by botiss biomaterials GmbH. The device was registered on October 26, 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.
Free DatabasePowered by Pure Global AIHSA Official DataCLASS D