Taiwan FDA registration d1bbf392e604223d282ef9c15836ceb0

"Heart drill" influenza virus antigen rapid test reagent (unsterilized)

TW: “心鑽” 流感病毒抗原快速檢驗試劑(未滅菌)

Taiwan·Risk Class 1·SYNTRON BIORESEARCH, INC.·Registered Jan 19, 2011 – Jan 19, 2016Cancelled

Registration details

Analysis ID: d1bbf392e604223d282ef9c15836ceb0
Customs Code: DHA04400982406

Company information

Manufacturer: SYNTRON BIORESEARCH, INC.
Manufacturer Country: United States
Authorized Representative: JOLEX INTERNATIONAL 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
Product Type (Level 2): C.3330 流感病毒血清試劑
Import Information: import

Dates and status

Registration Date: Jan 19, 2011
Expiry Date: Jan 19, 2016
Cancellation Date: Mar 29, 2017

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Heart drill" influenza virus antigen rapid test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d1bbf392e604223d282ef9c15836ceb0 and manufactured by SYNTRON BIORESEARCH, INC.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..

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