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“DiaSorin” Q Fever IFA IgG (Non-Sterile) - Taiwan Registration 16e9d7b25744aab4cdc80914b428dc2e

Access comprehensive regulatory information for “DiaSorin” Q Fever IFA IgG (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 16e9d7b25744aab4cdc80914b428dc2e and manufactured by DiaSorin Molecular LLC. The authorized representative in Taiwan is FENG CHI BIOTECH CORP..

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16e9d7b25744aab4cdc80914b428dc2e
Registration Details
Taiwan FDA Registration: 16e9d7b25744aab4cdc80914b428dc2e
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Device Details

“DiaSorin” Q Fever IFA IgG (Non-Sterile)
TW: “豐技”Q熱非直接免疫螢光抗體試驗--IgG(未滅菌)
Risk Class 1
MD

Registration Details

16e9d7b25744aab4cdc80914b428dc2e

Ministry of Health Medical Device Import No. 020400

DHA09402040001

Company Information

United States

Product Details

Limited to the first level identification range of Rickettsial serum reagent (C.3500) of the management method for medical devices.

C Immunology and microbiology devices

C3500 rickettsial serum reagent

Imported from abroad

Dates and Status

May 06, 2019

May 06, 2024