Taiwan FDA registration 51f101b441767ebddabdce2bd626553b
“Abbott” SHBG Reagent Kit (Non-Sterile)
TW: “亞培”性荷爾蒙結合球蛋白檢驗試劑組(未滅菌)
Taiwan·Risk Class 1·MD·BIOKIT S.A.·Registered Jan 31, 2019 – Jan 31, 2024ExpiredRegistration details
- Analysis ID
- 51f101b441767ebddabdce2bd626553b
- License Form
- Ministry of Health Medical Device Import No. 020085
- Customs Code
- DHA09402008506
Company information
- Manufacturer
- BIOKIT S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Limited to the first level identification range of the "testicular lipoketone test system (A.1680)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1680 Testicular Lipoketone Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 31, 2019
- Expiry Date
- Jan 31, 2024
About this record
Access comprehensive regulatory information for “Abbott” SHBG Reagent Kit (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 51f101b441767ebddabdce2bd626553b and manufactured by BIOKIT S.A.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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