Taiwan FDA registration 5cc861bc0ebd301522e3efef6fa8c230
LensHooke Sperm DNA Fragmentation Test Kit (Non-Sterile)
TW: 萊特兒精子染色試劑套組(未滅菌)
Taiwan·Risk Class 1·MD·BONRAYBIO CO., LTD.·Registered Dec 11, 2020 – Dec 11, 2025CancelledRegistration details
- Analysis ID
- 5cc861bc0ebd301522e3efef6fa8c230
- License Form
- Ministry of Health Medical Device Manufacturing No. 008723
Company information
- Manufacturer
- BONRAYBIO CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BONRAYBIO CO., LTD.
Product details
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B1850 Dyes and chemical solution dyes
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 11, 2020
- Expiry Date
- Dec 11, 2025
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for LensHooke Sperm DNA Fragmentation Test Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5cc861bc0ebd301522e3efef6fa8c230 and manufactured by BONRAYBIO CO., LTD.. The authorized representative in Taiwan is BONRAYBIO CO., LTD..
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