Taiwan FDA registration 97630f4e45310de2a23a34602601a177
"Baoling" pylori antigen rapid test reagent (unsterilized)
TW: “寶齡”幽門桿菌抗原快速檢測試劑(未滅菌)
Taiwan·Risk Class 1·Baoling Fujin Biotechnology Co., Ltd. Medical Equipment Factory·Registered Jun 16, 2006 – Jun 16, 2021CancelledRegistration details
- Analysis ID
- 97630f4e45310de2a23a34602601a177
- Customs Code
- DHY04300146002
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PANION & BF BIOTECH INC.
Product details
- 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
- Domestic
Dates and status
- Registration Date
- Jun 16, 2006
- Expiry Date
- Jun 16, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Baoling" pylori 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 97630f4e45310de2a23a34602601a177 and manufactured by Baoling Fujin Biotechnology Co., Ltd. Medical Equipment Factory. The authorized representative in Taiwan is PANION & BF BIOTECH INC..
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