Taiwan FDA registration 636535bccc8d0bb11e82967d967e3a2b
"Yingfang" anti-streptococcin O reagent (unsterilized)
TW: "瑩芳"抗鏈球菌素O試劑(未滅菌)
Taiwan·Risk Class 1·Yingfang Co., Ltd. Taichung Factory·Registered Nov 28, 2011 – Nov 28, 2021CancelledRegistration details
- Analysis ID
- 636535bccc8d0bb11e82967d967e3a2b
Company information
- Manufacturer
- Yingfang Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- Limit the management method of medical devices: Streptococcus is an exoenzyme reagent (C.3720) grade 1 identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3720 鏈球菌屬胞外酶試劑
- Import Information
- Domestic
Dates and status
- Registration Date
- Nov 28, 2011
- Expiry Date
- Nov 28, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Yingfang" anti-streptococcin O 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 636535bccc8d0bb11e82967d967e3a2b and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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