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Nofasiderence amoeba immunoglobulin G enzyme immunoassay kit (unsterilized) - Taiwan Registration f8db63680d3c4c62598304a4913782b3

Access comprehensive regulatory information for Nofasiderence amoeba immunoglobulin G enzyme immunoassay kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f8db63680d3c4c62598304a4913782b3 and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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f8db63680d3c4c62598304a4913782b3
Registration Details
Taiwan FDA Registration: f8db63680d3c4c62598304a4913782b3
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Device Details

Nofasiderence amoeba immunoglobulin G enzyme immunoassay kit (unsterilized)
TW: ่ซพๆณ•้ต็—ข็–พ้˜ฟ็ฑณๅทดๅ…็–ซ็ƒ่›‹็™ฝG้…ต็ด ๅ…็–ซๅˆ†ๆž่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f8db63680d3c4c62598304a4913782b3

DHA09402275509

Company Information

Product Details

Classification and Grading Management Measures for Medical Devices Limited to the Identification Range of the First Grade of Dysentery Amoeba Serological Reagent (C.3220).

C Immunology and microbiology

C.3220 ็—ข็–พ้˜ฟ็ฑณๅทด่ก€ๆธ…่ฉฆๅŠ‘

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Mar 10, 2022

Mar 10, 2027