Taiwan FDA registration 417466cbc0428b0f6a6b70a258e0bb5a
“DJO” Bone Growth Stimulator
TW: “迪捷歐”骨生長刺激器
Taiwan·Risk Class 3·MD·DJO, LLC·Registered Feb 12, 2019 – Feb 12, 2024ExpiredRegistration details
- Analysis ID
- 417466cbc0428b0f6a6b70a258e0bb5a
- License Form
- Ministry of Health Medical Device Import No. 031606
- Customs Code
- DHA05603160602
Company information
- Manufacturer
- DJO, LLC
- Manufacturer Country
- United States
- Authorized Representative
- LI-AN INTERNATIONAL BIOTECH CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O0002 Non-intrusive fracture fusion
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 12, 2019
- Expiry Date
- Feb 12, 2024
About this record
Access comprehensive regulatory information for “DJO” Bone Growth Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 417466cbc0428b0f6a6b70a258e0bb5a and manufactured by DJO, LLC. The authorized representative in Taiwan is LI-AN INTERNATIONAL BIOTECH CO., LTD..
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