Taiwan FDA registration 62218ade9a730df294131c21078f3700
“NEXOBIO ” Transcen Temporary Light Cured Resin
TW: “奈梭拜耳”傳勝臨時牙冠和牙橋樹脂
Taiwan·Risk Class 2·MD·NEXOBIO Co., Ltd.·Registered Jun 15, 2016 – Jun 15, 2026ExpiredRegistration details
- Analysis ID
- 62218ade9a730df294131c21078f3700
- License Form
- Ministry of Health Medical Device Import No. 028665
- Customs Code
- DHA05602866505
Company information
- Manufacturer
- NEXOBIO Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HSIN HUI MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3770 Temporary crown and bridge resin
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 15, 2016
- Expiry Date
- Jun 15, 2026
About this record
Access comprehensive regulatory information for “NEXOBIO ” Transcen Temporary Light Cured Resin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 62218ade9a730df294131c21078f3700 and manufactured by NEXOBIO Co., Ltd.. The authorized representative in Taiwan is HSIN HUI MEDICAL CO., LTD..
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