Taiwan FDA registration 1db780ff23bc28cf732241a2f90c7664
Streptococcus type A rapid test reagent (unsterilized)
TW: “凌越”A型鏈球菌快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·Lingyue Biomedical Co., Ltd. Taipei Factory·Registered Aug 26, 2013 – Aug 26, 2018CancelledRegistration details
- Analysis ID
- 1db780ff23bc28cf732241a2f90c7664
Company information
- Manufacturer
- Lingyue Biomedical Co., Ltd. Taipei Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Lingyue Biomedical Co., Ltd. Taipei Factory
Product details
- Intended Use
- Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3740 鏈球菌屬血清試劑
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 26, 2013
- Expiry Date
- Aug 26, 2018
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Streptococcus type A 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 1db780ff23bc28cf732241a2f90c7664 and manufactured by Lingyue Biomedical Co., Ltd. Taipei Factory. The authorized representative in Taiwan is Lingyue Biomedical Co., Ltd. Taipei Factory.
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