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Lingyue-specific immunoglobulin E immunofluorescence detection kit - Taiwan Registration 22e3ecdfcf709a6bf01f6b8f6232cad2

Access comprehensive regulatory information for Lingyue-specific immunoglobulin E immunofluorescence detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22e3ecdfcf709a6bf01f6b8f6232cad2 and manufactured by Lingyue Biomedical Co., Ltd. Taipei Factory. The authorized representative in Taiwan is Lingyue Biomedical Co., Ltd. Taipei Factory.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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22e3ecdfcf709a6bf01f6b8f6232cad2
Registration Details
Taiwan FDA Registration: 22e3ecdfcf709a6bf01f6b8f6232cad2
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Device Details

Lingyue-specific immunoglobulin E immunofluorescence detection kit
TW: ๅ‡Œ่ถŠ็‰น็•ฐๆ€งๅ…็–ซ็ƒ่›‹็™ฝEๅ…็–ซ่žขๅ…‰ๆชขๆธฌ่ฉฆๅŠ‘ๅฅ—็ต„
Risk Class 2

Registration Details

22e3ecdfcf709a6bf01f6b8f6232cad2

Company Information

Taiwan, Province of China

Product Details

This product is used for clinical in vitro semi-quantitative analysis of specific immunoglobulin E (specific IgE) content in human serum.

C Immunology and microbiology

C.5510 ๅ…็–ซ็ƒ่›‹็™ฝA,G,M,DๅŠEๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

Domestic

Dates and Status

Sep 10, 2012

Sep 10, 2027