Taiwan FDA registration c39756b61222027dda070f8273170502
“Dreve” Dynax Impression Materials
TW: “德瑞芙”蒂耐斯加成型印模材料
Registration details
- Analysis ID
- c39756b61222027dda070f8273170502
- License Form
- Ministry of Health Medical Device Import No. 035717
- Customs Code
- DHA05603571702
Company information
- Manufacturer
- DREVE DENTAMID GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MNM BIOTECHNOLOGY CO., LTD
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F3660 impression material
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 27, 2022
- Expiry Date
- Jul 27, 2027
About this record
Access comprehensive regulatory information for “Dreve” Dynax Impression Materials in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c39756b61222027dda070f8273170502 and manufactured by DREVE DENTAMID GMBH. The authorized representative in Taiwan is MNM BIOTECHNOLOGY 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