ABBOTT ARCHITECT DHEA-S (Non-Sterile)
Taiwan·Risk Class 1·MD·BIOKIT S.A.·Registered Oct 26, 2018 – Oct 26, 2028Active- Analysis ID
- 6325c00c4bf1ed7e36f1ad7fb0215acc
- License Form
- Ministry of Health Medical Device Import No. 019736
- Customs Code
- DHA09401973608
- Manufacturer
- BIOKIT S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Dehydroepiandrosterone (Free and Sulfur Salts) Test System (A.1245)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1245 Dehydroepiandrosterone (Free and Sulfur) Test System
- Import Information
- Imported from abroad
- Registration Date
- Oct 26, 2018
- Expiry Date
- Oct 26, 2028
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Access comprehensive regulatory information for ABBOTT ARCHITECT DHEA-S (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 6325c00c4bf1ed7e36f1ad7fb0215acc 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, 1 companies making similar products including BIOKIT S.A., and 1 recent registrations in the same category. 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.