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BioCer TiO2Mesh™ BRA Surgical Mesh Implant - HSA Registration DE0503957

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.

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CLASS C
DE0503957
BioCer TiO2Mesh™ BRA Surgical Mesh Implant
HSA Registration Number: DE0503957
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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.

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 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