Taiwan FDA registration 6212fce07fc2bb16499a6b9cc45f17e6

IF i-test Influenza A&B (non-sterile)

TW: 艾測A/B型流感快速檢驗試劑(未滅菌)

Taiwan·Risk Class 1·MD·Yingfang Co., Ltd. Taichung Factory·Registered Oct 17, 2017 – Oct 17, 2022Expired

Registration details

Analysis ID: 6212fce07fc2bb16499a6b9cc45f17e6
License Form: Ministry of Health Medical Device Manufacturing No. 006972

Company information

Manufacturer: Yingfang Co., Ltd. Taichung Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: IN FUNG CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3330 Influenza virus serum reagent
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 17, 2017
Expiry Date: Oct 17, 2022

About this record

Access comprehensive regulatory information for IF i-test Influenza A&B (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 6212fce07fc2bb16499a6b9cc45f17e6 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..

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