Taiwan FDA registration 501f48d64acef50693d890d9be764bca

Kaiwo Technology Helicobacter pylori test kit (IV)

TW: 開物科技幽門螺旋桿菌檢測試劑盒(IV)

Taiwan·Risk Class 1·SYNTRON BIORESEARCH INC.,·Registered Sep 26, 2007 – Sep 26, 2012Cancelled

Registration details

Analysis ID: 501f48d64acef50693d890d9be764bca
Customs Code: DHA04400617608

Company information

Manufacturer: SYNTRON BIORESEARCH INC.,
Manufacturer Country: United States
Authorized Representative: Kaiwu Technology Co., Ltd. Tainan Branch

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.0003 螺旋桿菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Sep 26, 2007
Expiry Date: Sep 26, 2012
Cancellation Date: May 05, 2014

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Kaiwo Technology Helicobacter pylori test kit (IV) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 501f48d64acef50693d890d9be764bca and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.

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