Taiwan FDA registration 9a52e8cba8a653d282046aeb75e705df
“NEXOBIO” Transeal F Pit and Fissure Sealant
TW: “奈塑寶”窩溝封閉劑
Taiwan·Risk Class 2·MD·NEXOBIO Co., Ltd.·Registered Feb 08, 2018 – Feb 08, 2023ExpiredRegistration details
- Analysis ID
- 9a52e8cba8a653d282046aeb75e705df
- License Form
- Ministry of Health Medical Device Import No. 030865
- Customs Code
- DHA05603086505
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)
- F3765 Pits and socket sealants and regulators
- 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” Transeal F Pit and Fissure Sealant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9a52e8cba8a653d282046aeb75e705df 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