Taiwan FDA registration 48a3b4b35ad3a2ae3094d22597cb6c41
Kaiwood OneStep H. Pylori Fecal Antigen Test (Non-Sterile)
TW: 開物 糞便胃幽門螺旋桿菌檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·SYNTRON BIORESEARCH INC.,·Registered Jun 30, 2015 – Jun 30, 2020CancelledRegistration details
- Analysis ID
- 48a3b4b35ad3a2ae3094d22597cb6c41
- License Form
- Ministry of Health Medical Device Import No. 015395
- Customs Code
- DHA09401539501
Company information
- Manufacturer
- SYNTRON BIORESEARCH INC.,
- Manufacturer Country
- United States
- Authorized Representative
- Kaiwu Technology Co., Ltd. Nanke Factory
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C0003 Helicobacter serological reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 30, 2015
- Expiry Date
- Jun 30, 2020
- Cancellation Date
- Jan 15, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Kaiwood OneStep H. Pylori Fecal Antigen Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 48a3b4b35ad3a2ae3094d22597cb6c41 and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Nanke 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