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“Diasorin” Chlamydia MIF IgM Kit (Non sterile) - Taiwan Registration 582f720e506172f155434d655b49bda4

Access comprehensive regulatory information for “Diasorin” Chlamydia MIF IgM 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 582f720e506172f155434d655b49bda4 and manufactured by DiaSorin Molecular LLC. The authorized representative in Taiwan is FENG CHI BIOTECH CORP..

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582f720e506172f155434d655b49bda4
Registration Details
Taiwan FDA Registration: 582f720e506172f155434d655b49bda4
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Device Details

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

Registration Details

582f720e506172f155434d655b49bda4

Ministry of Health Medical Device Import No. 020369

DHA09402036907

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