Taiwan FDA registration f091831ba3b11f0fd4d99babc8f89c3d
LensHooke Liquefaction Enzyme (Non-Sterile)
TW: 萊特兒液化酶(未滅菌)
Taiwan·Risk Class 1·MD·BONRAYBIO CO., LTD.·Registered Mar 20, 2020 – Mar 20, 2025ExpiredRegistration details
- Analysis ID
- f091831ba3b11f0fd4d99babc8f89c3d
- License Form
- Ministry of Health Medical Device Manufacturing No. 008245
Company information
- Manufacturer
- BONRAYBIO CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BONRAYBIO CO., LTD.
Product details
- Intended Use
- Limited to the preparation of semen samples, the use of chymotrypsin can break down proteins, accelerate the semen sample liquefaction time for subsequent in vitro testing.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9999 Other
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 20, 2020
- Expiry Date
- Mar 20, 2025
About this record
Access comprehensive regulatory information for LensHooke Liquefaction Enzyme (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 f091831ba3b11f0fd4d99babc8f89c3d and manufactured by BONRAYBIO CO., LTD.. The authorized representative in Taiwan is BONRAYBIO CO., LTD..
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