LZI Amphetamines 500 EIA Kit
- Analysis ID
- ccd4c02e21f43013cfc26de03ce61786
- License Form
- Ministry of Health Medical Device Import No. 031423
- Customs Code
- DHA05603142304
- 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 must 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
- Aug 15, 2018
- Expiry Date
- Aug 15, 2023
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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 ccd4c02e21f43013cfc26de03ce61786 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.