Taiwan FDA registration a626d5828001b53606ab4f52ee2d0e00
“DIO” Protem Implant System
TW: “帝歐”波登植體系統
Taiwan·Risk Class 3·MD·DIO CORPORATION·Registered Aug 18, 2015 – Aug 18, 2025ExpiredRegistration details
- Analysis ID
- a626d5828001b53606ab4f52ee2d0e00
- License Form
- Ministry of Health Medical Device Import No. 027636
- Customs Code
- DHA05602763606
Company information
- Manufacturer
- DIO CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DIO IMPLANT TAIWAN CORPORATION
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 18, 2015
- Expiry Date
- Aug 18, 2025
About this record
Access comprehensive regulatory information for “DIO” Protem 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 a626d5828001b53606ab4f52ee2d0e00 and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.
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