Taiwan FDA registration d36e42ee1e7ba392f27c73f794e33f50
“NEXOBIO” T Com Flow Flowable Composite Resin
TW: “奈塑寶”流動型複合樹脂
Taiwan·Risk Class 2·MD·NEXOBIO Co., Ltd.·Registered Feb 08, 2018 – Feb 08, 2023ExpiredRegistration details
- Analysis ID
- d36e42ee1e7ba392f27c73f794e33f50
- License Form
- Ministry of Health Medical Device Import No. 030864
- Customs Code
- DHA05603086403
Company information
- Manufacturer
- NEXOBIO Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- FIT DENTAL INTERNATIONAL TRADE 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)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 08, 2018
- Expiry Date
- Feb 08, 2023
About this record
Access comprehensive regulatory information for “NEXOBIO” T Com Flow Flowable Composite Resin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d36e42ee1e7ba392f27c73f794e33f50 and manufactured by NEXOBIO Co., Ltd.. The authorized representative in Taiwan is FIT DENTAL INTERNATIONAL TRADE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices