LZI Amphetamines 500 EIA Kit
Taiwan·Risk Class 2·MD·LIN-ZHI INTERNATIONAL, INC·Registered Nov 21, 2018 – Nov 21, 2028Active- Analysis ID
- 14980f460b2117d055c8c9dffedcdf36
- License Form
- Ministry of Health Medical Device Import No. 031803
- Customs Code
- DHA05603180301
- Manufacturer
- LIN-ZHI INTERNATIONAL, INC
- Manufacturer Country
- United States
- Authorized Representative
- TAIWAN ADVANCE BIO-PHARMACEUTICAL INC.
- Intended Use
- This product is used for the qualitative or semi-quantitative determination of amphetamines and methamphetamines in human urine, and needs to be used with an automated biochemical analyzer with a threshold of 500ng/mL (corrected by d-methamphetamine).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A3100 Amphetamine Test System
- Import Information
- Imported from abroad
- Registration Date
- Nov 21, 2018
- Expiry Date
- Nov 21, 2028
Top companies providing products similar to "LZI Amphetamines 500 EIA Kit"
Recently registered similar products
Access comprehensive regulatory information for LZI Amphetamines 500 EIA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14980f460b2117d055c8c9dffedcdf36 and manufactured by LIN-ZHI INTERNATIONAL, INC. The authorized representative in Taiwan is TAIWAN ADVANCE BIO-PHARMACEUTICAL INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LIN-ZHI INTERNATIONAL, INC, 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.