Taiwan FDA registration ed73195747ba1f6bd9d0563bf07d9e15
"Cottman" Beates shunt
TW: “柯特曼”貝特斯分流器
Taiwan·Risk Class 2·CODMAN & SHURTLEFF,INC.·Registered Feb 01, 2011 – Feb 01, 2016CancelledRegistration details
- Analysis ID
- ed73195747ba1f6bd9d0563bf07d9e15
- Customs Code
- DHA00602205201
Company information
- Manufacturer
- CODMAN & SHURTLEFF,INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5550 Central nervous system fluid diverter and its components
- Import Information
- import
Dates and status
- Registration Date
- Feb 01, 2011
- Expiry Date
- Feb 01, 2016
- Cancellation Date
- Aug 01, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Cottman" Beates shunt in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed73195747ba1f6bd9d0563bf07d9e15 and manufactured by CODMAN & SHURTLEFF,INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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