Taiwan FDA registration a3faa0b6537852a575006fda1d230d67
"Metifix" non-powered neurosurgical instruments (unsterilized)
TW: "梅帝菲克斯" 非動力式神經外科用器械 (未滅菌)
Taiwan·Risk Class 1·MEDIFLEX DIVISION OF FLEXBAR MACHINE CORPORATION·Registered Apr 14, 2006 – Apr 14, 2021CancelledRegistration details
- Analysis ID
- a3faa0b6537852a575006fda1d230d67
- Customs Code
- DHA04400388305
Company information
- Manufacturer
- MEDIFLEX DIVISION OF FLEXBAR MACHINE CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Liren Equipment Factory Co., Ltd
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
- Apr 14, 2006
- Expiry Date
- Apr 14, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Metifix" 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 a3faa0b6537852a575006fda1d230d67 and manufactured by MEDIFLEX DIVISION OF FLEXBAR MACHINE CORPORATION. The authorized representative in Taiwan is Liren Equipment Factory Co., Ltd.
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