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Longteng K in vitro reagent group - Taiwan Registration b35d99e84518cef5611497fd14694b2e

Access comprehensive regulatory information for Longteng K in vitro reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b35d99e84518cef5611497fd14694b2e and manufactured by Longteng Biotechnology Co., Ltd. new market factory. The authorized representative in Taiwan is Longteng Biotechnology Co., Ltd. new market factory.

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b35d99e84518cef5611497fd14694b2e
Registration Details
Taiwan FDA Registration: b35d99e84518cef5611497fd14694b2e
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Device Details

Longteng K in vitro reagent group
TW: ้พ้จฐKไป–ๅ‘ฝ้ซ”ๅค–่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

b35d99e84518cef5611497fd14694b2e

Company Information

Product Details

Qualitative detection of Khimmine and its metabolites in human urine.

A Clinical chemistry and clinical toxicology

A.0001 ่‹ฏ็’ฐๅˆฉๅฎš่ฉฆ้ฉ—็ณป็ตฑ

Domestic

Dates and Status

Feb 18, 2020

Feb 18, 2030