Taiwan FDA registration 0678a47f66324ea527d870d04a05d317
“HumanTech” Ratioplant Dental Implant System
TW: “賽門鐵克”牙科植體系統
Taiwan·Risk Class 3·MD·HUMANTECH GERMANY GMBH·Registered Aug 03, 2016 – Aug 03, 2021ExpiredRegistration details
- Analysis ID
- 0678a47f66324ea527d870d04a05d317
- License Form
- Ministry of Health Medical Device Import No. 028709
- Customs Code
- DHA05602870902
Company information
- Manufacturer
- HUMANTECH GERMANY GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- DENTAL EASE TECHNOLOGY 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)
- F3640 Bone explants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 03, 2016
- Expiry Date
- Aug 03, 2021
About this record
Access comprehensive regulatory information for “HumanTech” Ratioplant Dental Implant System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0678a47f66324ea527d870d04a05d317 and manufactured by HUMANTECH GERMANY GMBH. The authorized representative in Taiwan is DENTAL EASE TECHNOLOGY 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