Taiwan FDA registration fdb09382bfe77bbb9c737bb2ccbe12dd
"Bosch" tracheal fixture (unsterilized)
TW: "波希"氣管管路固定裝置(未滅菌)
Taiwan·Risk Class 1·POSEY MEXICO·Registered Oct 12, 2012 – Oct 12, 2022CancelledRegistration details
- Analysis ID
- fdb09382bfe77bbb9c737bb2ccbe12dd
- Customs Code
- DHA04401224602
Company information
- Manufacturer
- POSEY MEXICO
- Manufacturer Country
- Mexico
- Authorized Representative
- NSH MEDICAL CORP.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5770 氣管管路固定裝置
- Import Information
- import
Dates and status
- Registration Date
- Oct 12, 2012
- Expiry Date
- Oct 12, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bosch" tracheal fixture (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fdb09382bfe77bbb9c737bb2ccbe12dd and manufactured by POSEY MEXICO. The authorized representative in Taiwan is NSH MEDICAL CORP..
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