Taiwan FDA registration d1ce1c8288ebfead84c8d89fdaf1a6c9
"Keai Fusen" Miller Non-powered neurosurgical instruments (unsterilized)
TW: "客愛福生" 米樂 非動力式神經外科用器械 (未滅菌)
Taiwan·Risk Class 1·CAREFUSION·Registered Nov 08, 2011 – Nov 08, 2021CancelledRegistration details
- Analysis ID
- d1ce1c8288ebfead84c8d89fdaf1a6c9
- Customs Code
- DHA04401103102
Company information
- Manufacturer
- CAREFUSION
- Manufacturer Country
- United States
- Authorized Representative
- CHAMPION MEDICAL CORPORATION
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4535 非動力式神經外科用器械
- Import Information
- import
Dates and status
- Registration Date
- Nov 08, 2011
- Expiry Date
- Nov 08, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Keai Fusen" Miller Non-powered neurosurgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d1ce1c8288ebfead84c8d89fdaf1a6c9 and manufactured by CAREFUSION. The authorized representative in Taiwan is CHAMPION MEDICAL CORPORATION.
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