Taiwan FDA registration a37ff6d14821d24c1b1eb13cfa050363

"Sodi" influenza virus antigen rapid test reagent (unsterilized)

TW: “速帝”流感病毒抗原快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·STANDARD DIAGNOSTICS, INC.·Registered Aug 12, 2010 – Aug 12, 2015Cancelled

Registration details

Analysis ID: a37ff6d14821d24c1b1eb13cfa050363
Customs Code: DHA04400908701

Company information

Manufacturer: STANDARD DIAGNOSTICS, INC.
Manufacturer Country: Korea, Republic of
Authorized Representative: Ariel Health Inc

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: Aug 12, 2010
Expiry Date: Aug 12, 2015
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Sodi" 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 a37ff6d14821d24c1b1eb13cfa050363 and manufactured by STANDARD DIAGNOSTICS, INC.. The authorized representative in Taiwan is Ariel Health Inc.

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