Taiwan FDA registration d520c32bf9ced6b5642d10a77202a724
"WAKO" Lipase Test (Non-Sterile)
TW: "和光"脂肪分解酵素試劑(未滅菌)
Taiwan·Risk Class 1·MD·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Mar 27, 2014 – Mar 27, 2024ExpiredRegistration details
- Analysis ID
- d520c32bf9ced6b5642d10a77202a724
- License Form
- Ministry of Health Medical Device Import No. 013989
- Customs Code
- DHA09401398907
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Limited to the first level identification range of the Lipolytic Enzyme Test System (A.1465) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1465 Lipolytic enzyme test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 27, 2014
- Expiry Date
- Mar 27, 2024
About this record
Access comprehensive regulatory information for "WAKO" Lipase Test (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 d520c32bf9ced6b5642d10a77202a724 and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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