Taiwan FDA registration 1afbaa1bba097bdd90bfa40219b856cf
Quick Result hCG Pregnancy Test
TW: 快適得驗孕試劑
Taiwan·Risk Class 2·MD·Longteng Biotechnology Co., Ltd. new market factory·Registered Jan 08, 2019 – Oct 26, 2028ActiveRegistration details
- Analysis ID
- 1afbaa1bba097bdd90bfa40219b856cf
- License Form
- Ministry of Health Medical Device Manufacturing No. 006272
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KING WARE ENTERPRISE CORP.
Product details
- Intended Use
- This product qualitatively detects human chorionic gonadotropins in human urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1155 Human chorionic gonadotropin test system
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Jan 08, 2019
- Expiry Date
- Oct 26, 2028
About this record
Access comprehensive regulatory information for Quick Result hCG Pregnancy Test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1afbaa1bba097bdd90bfa40219b856cf and manufactured by Longteng Biotechnology Co., Ltd. new market factory. The authorized representative in Taiwan is KING WARE ENTERPRISE CORP..
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