Taiwan FDA registration b53efaa7f0c04560e41e6e86c6d5dad9
“T&R” Nasal Mesh
TW: “媞雅”鼻骨修補網片
Taiwan·Risk Class 2·MD·T&R Biofab Co., Ltd.·Registered Jan 14, 2021 – Jan 14, 2026ExpiredRegistration details
- Analysis ID
- b53efaa7f0c04560e41e6e86c6d5dad9
- License Form
- Ministry of Health Medical Device Import No. 034261
- Customs Code
- DHA05603426106
Company information
- Manufacturer
- T&R Biofab Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- PRIMESTAR MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5300 Methyl methacrylate for craniomatomy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 14, 2021
- Expiry Date
- Jan 14, 2026
About this record
Access comprehensive regulatory information for “T&R” Nasal Mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b53efaa7f0c04560e41e6e86c6d5dad9 and manufactured by T&R Biofab Co., Ltd.. The authorized representative in Taiwan is PRIMESTAR MEDICAL CO., LTD..
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