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"WAKO" Lipase Test (Non-Sterile) - Taiwan Registration d520c32bf9ced6b5642d10a77202a724

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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d520c32bf9ced6b5642d10a77202a724
Registration Details
Taiwan FDA Registration: d520c32bf9ced6b5642d10a77202a724
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Device Details

"WAKO" Lipase Test (Non-Sterile)
TW: "ๅ’Œๅ…‰"่„‚่‚ชๅˆ†่งฃ้…ต็ด ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d520c32bf9ced6b5642d10a77202a724

Ministry of Health Medical Device Import No. 013989

DHA09401398907

Company Information

Product Details

Limited to the first level identification range of the Lipolytic Enzyme Test System (A.1465) of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1465 Lipolytic enzyme test system

Imported from abroad

Dates and Status

Mar 27, 2014

Mar 27, 2024