Taiwan FDA registration c33019f0eaaad550f14eb3e89ea06c7d
TOYOBO AUTOMATED URINE CELL ANALYZER USCANNER premio
TW: 東洋紡尿液沉渣細胞自動染色電腦影像分析儀
Taiwan·Risk Class 2·MD·TOYOBO CO., LTD.·Registered Jul 06, 2020 – Jul 06, 2025ExpiredRegistration details
- Analysis ID
- c33019f0eaaad550f14eb3e89ea06c7d
- License Form
- Ministry of Health Medical Device Import No. 033502
- Customs Code
- DHA05603350200
Company information
- Manufacturer
- TOYOBO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- AMESDATA BIOTECH CO., LTD.
Product details
- Intended Use
- This product uses photography to group and semi-quantitatively count urine sediment cells by imaging analysis.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B5220 automatically differentiates cell counters
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 06, 2020
- Expiry Date
- Jul 06, 2025
About this record
Access comprehensive regulatory information for TOYOBO AUTOMATED URINE CELL ANALYZER USCANNER premio in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c33019f0eaaad550f14eb3e89ea06c7d and manufactured by TOYOBO CO., LTD.. The authorized representative in Taiwan is AMESDATA BIOTECH CO., LTD..
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