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"Ruimai" dysentery amoeba detection reagent (non-sterilized) - Taiwan Registration a4a49221572e2986f351d2a790032e0c

Access comprehensive regulatory information for "Ruimai" dysentery amoeba detection reagent (non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a4a49221572e2986f351d2a790032e0c and manufactured by OXOID LIMITED;; Remel Europe Limited. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE CO., LTD..

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a4a49221572e2986f351d2a790032e0c
Registration Details
Taiwan FDA Registration: a4a49221572e2986f351d2a790032e0c
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Device Details

"Ruimai" dysentery amoeba detection reagent (non-sterilized)
TW: "้Šณ้‚" ็—ข็–พ้˜ฟ็ฑณๅทดๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

a4a49221572e2986f351d2a790032e0c

DHA09402359801

Company Information

United Kingdom

Product Details

Limited to the first level of identification of dysentery amoeba serum reagent (C.3220) in the Administrative Measures for the Classification and Grading of Medical Devices.

C Immunology and microbiology

C.3220 ็—ข็–พ้˜ฟ็ฑณๅทด่ก€ๆธ…่ฉฆๅŠ‘

Input;; QMS/QSD

Dates and Status

Sep 06, 2024

Sep 06, 2029