Taiwan FDA registration d14cc0ded93ea2825cb8b0f394ff879c
"Jinggang" posterior spinal fixator system
TW: “精剛”脊椎後方固定器系統
Taiwan·Risk Class 2·S-TECH CORP.·Registered May 12, 2008 – May 12, 2013CancelledRegistration details
- Analysis ID
- d14cc0ded93ea2825cb8b0f394ff879c
- Customs Code
- DHY00500243501
Company information
- Manufacturer
- S-TECH CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- S-TECH CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3070 椎弓螺釘系統
- Import Information
- Domestic
Dates and status
- Registration Date
- May 12, 2008
- Expiry Date
- May 12, 2013
- Cancellation Date
- Jun 03, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jinggang" posterior spinal fixator system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d14cc0ded93ea2825cb8b0f394ff879c and manufactured by S-TECH CORP.. The authorized representative in Taiwan is S-TECH CORP..
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