Taiwan FDA registration e885f230f78dd8158012b3898ab9eb5e
Vitron cranial bone fixation system
TW: 威創顱顏骨固定系統
Taiwan·Risk Class 2·INTAI TECHNOLOGY CORP.·Registered Sep 03, 2010 – Aug 05, 2015CancelledRegistration details
- Analysis ID
- e885f230f78dd8158012b3898ab9eb5e
- Customs Code
- DHY00500308709
Company information
- Manufacturer
- INTAI TECHNOLOGY CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WILTROM 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.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Sep 03, 2010
- Expiry Date
- Aug 05, 2015
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Vitron cranial bone fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e885f230f78dd8158012b3898ab9eb5e and manufactured by INTAI TECHNOLOGY CORP.. The authorized representative in Taiwan is WILTROM CO., LTD..
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