Taiwan FDA registration f6c14fd022d38e655d057ae849e5774c
“Dentis” Cleanlant I-FIX Implant System
TW: “登特司”克林蘭特愛菲司牙科植體系統
Taiwan·Risk Class 3·MD·Dentis Co., Ltd.·Registered Apr 27, 2016 – Apr 27, 2026ExpiredRegistration details
- Analysis ID
- f6c14fd022d38e655d057ae849e5774c
- License Form
- Ministry of Health Medical Device Import No. 028551
- Customs Code
- DHA05602855103
Company information
- Manufacturer
- Dentis Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- TAIWAN DENTIS DENTAL 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
- Apr 27, 2016
- Expiry Date
- Apr 27, 2026
About this record
Access comprehensive regulatory information for “Dentis” Cleanlant I-FIX 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 f6c14fd022d38e655d057ae849e5774c and manufactured by Dentis Co., Ltd.. The authorized representative in Taiwan is TAIWAN DENTIS DENTAL TECHNOLOGY CO., LTD..
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