Taiwan FDA registration 2016e2029f2779d03fcefc57464e71e0
“Pasesa” Non-invasive Vascular Screening Device
TW: “帕醫生”非侵入性血管檢測儀
Taiwan·Risk Class 2·MD·SINTAI OPTICAL(SHEN ZHEN)CO., LTD.·Registered Jan 06, 2021 – Jan 06, 2026ExpiredRegistration details
- Analysis ID
- 2016e2029f2779d03fcefc57464e71e0
- License Form
- Ministry of Health Medical Device Land Transport No. 001193
- Customs Code
- DHA09200119302
Company information
- Manufacturer
- SINTAI OPTICAL(SHEN ZHEN)CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- GENEWAY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1130 Non-invasive blood pressure measurement system
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Jan 06, 2021
- Expiry Date
- Jan 06, 2026
About this record
Access comprehensive regulatory information for “Pasesa” Non-invasive Vascular Screening Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2016e2029f2779d03fcefc57464e71e0 and manufactured by SINTAI OPTICAL(SHEN ZHEN)CO., LTD.. The authorized representative in Taiwan is GENEWAY CO., LTD..
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