Taiwan FDA registration 861ba9d6c95c538c5ec5d0d7e7cfb5ff
"Sanyang" arterial vascular detector
TW: “山陽”動脈血管檢測儀
Taiwan·Risk Class 2·SANYOSEIKO CO., LTD.·Registered Dec 19, 2019 – Dec 19, 2029ActiveRegistration details
- Analysis ID
- 861ba9d6c95c538c5ec5d0d7e7cfb5ff
- Customs Code
- DHA05603306909
Company information
- Manufacturer
- SANYOSEIKO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH 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.1130.
- Import Information
- import
Dates and status
- Registration Date
- Dec 19, 2019
- Expiry Date
- Dec 19, 2029
About this record
Access comprehensive regulatory information for "Sanyang" arterial vascular detector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 861ba9d6c95c538c5ec5d0d7e7cfb5ff and manufactured by SANYOSEIKO CO., LTD.. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
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