Taiwan FDA registration c90cc778c9c7b8dcc78e3d814a27d206
"Aibang" single-step Helicobacter pylori (feces) antigen rapid test reagent (unsterilized)
TW: “艾邦”單一步驟幽門螺旋桿菌(糞便)抗原快速檢測試劑(未滅菌)
Registration details
- Analysis ID
- c90cc778c9c7b8dcc78e3d814a27d206
- Customs Code
- DHA04600157003
Company information
- Manufacturer
- ABON BIOPHARM (HANGZHOU) CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
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
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 16, 2012
- Expiry Date
- Jan 16, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aibang" single-step Helicobacter pylori (feces) 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 c90cc778c9c7b8dcc78e3d814a27d206 and manufactured by ABON BIOPHARM (HANGZHOU) CO., LTD. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices