Taiwan FDA registration 6aa66a72790bd93a10257478b8037f4e
Blue Angel pregnancy rapid test reagent series
TW: 藍天使懷孕快速檢驗試劑系列
Taiwan·Risk Class 2·Longteng Biotechnology Co., Ltd·Registered Mar 31, 2008 – Mar 31, 2013CancelledRegistration details
- Analysis ID
- 6aa66a72790bd93a10257478b8037f4e
- Customs Code
- DHY00500258000
Company information
- Manufacturer
- Longteng Biotechnology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Xile Enterprises Limited
Product details
- Intended Use
- Qualitative testing of human pilionic gonadotropins.
- 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
- Mar 31, 2008
- Expiry Date
- Mar 31, 2013
- Cancellation Date
- Jun 02, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Blue Angel pregnancy rapid test reagent series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6aa66a72790bd93a10257478b8037f4e and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is Xile Enterprises Limited.
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.
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