Taiwan FDA registration 07539d7f180bb2bab1b85f1862b4b4f8
"Jintai" torso device (unsterilized)
TW: "進泰" 軀幹裝具 (未滅菌)
Taiwan·Risk Class 1·NEOPLEX INDUSTRIAL CO., LTD.·Registered Mar 18, 2014 – Mar 18, 2019CancelledRegistration details
- Analysis ID
- 07539d7f180bb2bab1b85f1862b4b4f8
Company information
- Manufacturer
- NEOPLEX INDUSTRIAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- NEOPLEX INDUSTRIAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3490 Torso mounting
- Import Information
- Domestic
Dates and status
- Registration Date
- Mar 18, 2014
- Expiry Date
- Mar 18, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jintai" torso device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 07539d7f180bb2bab1b85f1862b4b4f8 and manufactured by NEOPLEX INDUSTRIAL CO., LTD.. The authorized representative in Taiwan is NEOPLEX INDUSTRIAL CO., LTD..
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