Taiwan FDA registration 52cbddc1649f5bb3da505d76beece3e5

Kaiwu Influenza Type A and B Kits

TW: 開物科技流行性感冒A型及B型試劑盒

Taiwan·Risk Class 1·SYNTRON BIORESEARCH INC.,·Registered Feb 25, 2008 – Feb 25, 2013Cancelled

Registration details

Analysis ID: 52cbddc1649f5bb3da505d76beece3e5
Customs Code: DHA04400653803

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 "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: Feb 25, 2008
Expiry Date: Feb 25, 2013
Cancellation Date: Jun 11, 2015

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Kaiwu Influenza Type A and B Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 52cbddc1649f5bb3da505d76beece3e5 and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.

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