Singapore HSA registration DE0503957
BioCer TiO2Mesh™ BRA Surgical Mesh Implant
Device classification
- Device Class
- CLASS C
- Medical Speciality Area
- General & Plastic Surgery
Registration information
- Registration Number
- DE0503957
- Registration Date
- December 19, 2019
- Change Notification Approval Date
- February 11, 2025
- Retention Due Date
- December 18, 2025
Product description
TiO2Mesh™ BRA is a surgical mesh implant for the support, reinforcement and bridging of body’s own tissue in reconstructive and medically indicated plastic-aesthetic breast surgery.
Product Owner
- Short Name
- BioCer Entwicklungs
- Address
- Ludwig-Thoma-Staϐe 36 c, 95447 Bayreuth, GERMANY
Registrant
- Address
- 23 NEW INDUSTRIAL ROAD, SOLSTICE BUSINESS CENTER, #03-08, SINGAPORE 536209
Importer
- Address
- 23 NEW INDUSTRIAL ROAD, SOLSTICE BUSINESS CENTER, #03-08, SINGAPORE 536209
Model information
- Model Name(s)
- TiO2Mesh™ BRA Surgical Mesh Implant Small TiO2Mesh™ BRA Surgical Mesh Implant Medium TiO2Mesh™ BRA Surgical Mesh Implant Large TiO2Mesh™ BRA light Surgical Mesh Implant Small TiO2Mesh™ BRA light Surgical Mesh Implant Medium TiO2Mesh™ BRA light Surgical Mesh Implant Large
- Model Identifier(s)
- MFP511 MFP512 MFP513 MFP611 MFP612 MFP613
About this record
Access comprehensive regulatory information for BioCer TiO2Mesh™ BRA Surgical Mesh Implant in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0503957 and owned by BioCer Entwicklungs-GmbH. The device was registered on December 19, 2019.
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 C