Taiwan FDA registration 6ff0dff14cc5d1de3050d2e7e868d19f
"Artis" vascular examiner
TW: "亞提斯"血管檢查儀
Taiwan·Risk Class 2·ATYS MEDICAL·Registered Aug 08, 2006 – Aug 08, 2021CancelledRegistration details
- Analysis ID
- 6ff0dff14cc5d1de3050d2e7e868d19f
- Customs Code
- DHA00601697600
Company information
- Manufacturer
- ATYS MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- NIEN TAI MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2780 液壓.、氣壓或光電式體積描記器
- Import Information
- import
Dates and status
- Registration Date
- Aug 08, 2006
- Expiry Date
- Aug 08, 2021
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Artis" vascular examiner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ff0dff14cc5d1de3050d2e7e868d19f and manufactured by ATYS MEDICAL. The authorized representative in Taiwan is NIEN TAI MEDICAL INSTRUMENTS CO., LTD..
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