Taiwan FDA registration 6a3daec8b1a02244691c8b2a195f20fe
Kaiwo Technology Type A Streptococcus Test Kit (Unsterilized)
TW: 開物科技A型鏈球菌檢測試劑盒(未滅菌)
Taiwan·Risk Class 1·SYNTRON BIORESEARCH INC.,·Registered Oct 04, 2007 – Oct 04, 2017CancelledRegistration details
- Analysis ID
- 6a3daec8b1a02244691c8b2a195f20fe
- Customs Code
- DHA04400619907
Company information
- Manufacturer
- SYNTRON BIORESEARCH INC.,
- Manufacturer Country
- United States
- Authorized Representative
- Kaiwu Technology Co., Ltd. Tainan Branch
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
- import
Dates and status
- Registration Date
- Oct 04, 2007
- Expiry Date
- Oct 04, 2017
- Cancellation Date
- Nov 22, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Kaiwo Technology Type A Streptococcus Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6a3daec8b1a02244691c8b2a195f20fe and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.
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