Taiwan FDA registration e09a595060205209630895040de6b590
“Dreve” Regofix Bite Registration Material
TW: “德瑞芙”瑞格菲斯咬合記錄材
Taiwan·Risk Class 2·MD·Dreve Dentamid GmbH·Registered Jun 23, 2017 – Jun 23, 2027ActiveRegistration details
- Analysis ID
- e09a595060205209630895040de6b590
- License Form
- Ministry of Health Medical Device Import No. 029913
- Customs Code
- DHA05602991303
Company information
- Manufacturer
- Dreve Dentamid GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- MNM BIOTECHNOLOGY 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)
- F3660 impression material
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 23, 2017
- Expiry Date
- Jun 23, 2027
About this record
Access comprehensive regulatory information for “Dreve” Regofix Bite Registration Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e09a595060205209630895040de6b590 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