Taiwan FDA registration 1812f0b0d732d718da003254de7d6cfa
"Difu Spine" Fronti Scoliosis Correction System
TW: "帝富脊椎" 佛朗帝脊柱側彎前方矯治系統
Taiwan·Risk Class 2·DEPUY SPINE, INC.·Registered Feb 25, 2003 – Feb 25, 2018CancelledRegistration details
- Analysis ID
- 1812f0b0d732d718da003254de7d6cfa
- Customs Code
- DHA00601022707
Company information
- Manufacturer
- DEPUY SPINE, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Feb 25, 2003
- Expiry Date
- Feb 25, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Difu Spine" Fronti Scoliosis Correction System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1812f0b0d732d718da003254de7d6cfa and manufactured by DEPUY SPINE, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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