Taiwan FDA registration 67b22d638b3e2fb496a79a6e25aa7bf8
“Dentis” i-Clean OneQ-SL Implant System
TW: “登特司”愛客林萬客牙科植體系統
Taiwan·Risk Class 3·MD·Dentis Co., Ltd.·Registered Aug 11, 2016 – Aug 11, 2021CancelledRegistration details
- Analysis ID
- 67b22d638b3e2fb496a79a6e25aa7bf8
- License Form
- Ministry of Health Medical Device Import No. 028725
- Customs Code
- DHA05602872500
Company information
- Manufacturer
- Dentis Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- TAIWAN DENTIS DENTAL TECHNOLOGY CO., LTD.
Product details
- 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 11, 2016
- Expiry Date
- Aug 11, 2021
- Cancellation Date
- Aug 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Dentis” i-Clean OneQ-SL 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 67b22d638b3e2fb496a79a6e25aa7bf8 and manufactured by Dentis Co., Ltd.. The authorized representative in Taiwan is TAIWAN DENTIS DENTAL 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