Taiwan FDA registration 0e9705cfde3e5c5d0354cd37589b10d9
Bafang rapid pregnancy test reagent
TW: 八方快速驗孕試劑
Taiwan·Risk Class 2·Lianshang Biotechnology Co., Ltd. Wugu Factory·Registered Aug 09, 2006 – Aug 09, 2011CancelledRegistration details
- Analysis ID
- 0e9705cfde3e5c5d0354cd37589b10d9
- Customs Code
- DHY00500216702
Company information
- Manufacturer
- Lianshang Biotechnology Co., Ltd. Wugu Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Whole Valley Biotechnology Co., Ltd
Product details
- Intended Use
- Immunochromatography was used to qualitatively detect human placental chorionic gonadal hormone (threshold 25 mIU/mL) in urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 09, 2006
- Expiry Date
- Aug 09, 2011
- Cancellation Date
- Oct 25, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Bafang rapid pregnancy test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0e9705cfde3e5c5d0354cd37589b10d9 and manufactured by Lianshang Biotechnology Co., Ltd. Wugu Factory. The authorized representative in Taiwan is Whole Valley Biotechnology Co., Ltd.
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