Taiwan FDA registration 1083e5f910076a83ea1177d16f1df6b6
"Acetrich" neurosurgical instruments (unsterilized)
TW: “亞氏” 神經外科手術器械（未滅菌）
Taiwan·Risk Class 1·AESCULAP AG·Registered Mar 28, 2011 – Mar 28, 2016CancelledRegistration details
- Analysis ID
- 1083e5f910076a83ea1177d16f1df6b6
- Customs Code
- DHA04401009204
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- Jiatai Medical Equipment 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
- Mar 28, 2011
- Expiry Date
- Mar 28, 2016
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Acetrich" 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 1083e5f910076a83ea1177d16f1df6b6 and manufactured by AESCULAP AG. The authorized representative in Taiwan is Jiatai Medical Equipment Co., Ltd.
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