Taiwan FDA registration 85e403829a43843e0cf8ace5dfa48b54
Kaiwo Technology Helicobacter pylori antigen detection kit (II) (unsterilized)
TW: 開物科技幽門螺旋桿菌抗原檢測試劑盒(II)(未滅菌)
Taiwan·Risk Class 1·SYNTRON BIORESEARCH INC.,·Registered Sep 26, 2007 – Sep 26, 2017CancelledRegistration details
- Analysis ID
- 85e403829a43843e0cf8ace5dfa48b54
- Customs Code
- DHA04400617700
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, 2017
- Cancellation Date
- Nov 22, 2019
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 antigen detection kit (II) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 85e403829a43843e0cf8ace5dfa48b54 and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.
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