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“Diasorin” Chlamydia MIF IgG Kit (Non sterile) - Taiwan Registration c45fe725058d5fca7e24737f01bbc91e

Access comprehensive regulatory information for “Diasorin” Chlamydia MIF IgG Kit (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 c45fe725058d5fca7e24737f01bbc91e and manufactured by DiaSorin Molecular LLC. The authorized representative in Taiwan is FENG CHI BIOTECH CORP..

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c45fe725058d5fca7e24737f01bbc91e
Registration Details
Taiwan FDA Registration: c45fe725058d5fca7e24737f01bbc91e
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Device Details

“Diasorin” Chlamydia MIF IgG Kit (Non sterile)
TW: “豐技”披衣菌微免疫螢光IgG試驗套組 (未滅菌)
Risk Class 1
MD

Registration Details

c45fe725058d5fca7e24737f01bbc91e

Ministry of Health Medical Device Import No. 020368

DHA09402036805

Company Information

United States

Product Details

Limited to the first level identification range of Chlamydomydia serum reagent (C.3120) of medical device management methods.

C Immunology and microbiology devices

C3120 Chlamydia serum reagent

Imported from abroad

Dates and Status

Apr 25, 2019

Apr 25, 2024