Taiwan FDA registration c25a77300834c5999224288135d0f088
"Difu Xindis" Webis vertebral stent inflatable system
TW: “帝富信迪思”威比士椎體支架充氣系統
Taiwan·Risk Class 2·PEROUSE MEDICAL·Registered Nov 30, 2023 – Nov 30, 2028ActiveRegistration details
- Analysis ID
- c25a77300834c5999224288135d0f088
- Customs Code
- DHA05603686203
Company information
- Manufacturer
- PEROUSE MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.9999 Other; N.3060 Spine Correction Fixation Between the Vertebrae
- Import Information
- import
Dates and status
- Registration Date
- Nov 30, 2023
- Expiry Date
- Nov 30, 2028
About this record
Access comprehensive regulatory information for "Difu Xindis" Webis vertebral stent inflatable system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c25a77300834c5999224288135d0f088 and manufactured by PEROUSE MEDICAL. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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