Taiwan FDA registration 10c55463691c56aef8f50dbf90a95d3d
"Chang'an" cervical intervertebral fusion device
TW: “長安”頸椎椎間融合器
Taiwan·Risk Class 2·WELLONG INSTRUMENTS CO., LTD.·Registered Jun 24, 2008 – Jun 24, 2028ActiveRegistration details
- Analysis ID
- 10c55463691c56aef8f50dbf90a95d3d
- Customs Code
- DHY00500245405
Company information
- Manufacturer
- WELLONG INSTRUMENTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WELLONG INSTRUMENTS CO., LTD.
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.3060 椎體間之脊椎矯正固定物
- Import Information
- Domestic
Dates and status
- Registration Date
- Jun 24, 2008
- Expiry Date
- Jun 24, 2028
About this record
Access comprehensive regulatory information for "Chang'an" cervical intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 10c55463691c56aef8f50dbf90a95d3d and manufactured by WELLONG INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..
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