Taiwan FDA registration 5b5868963c0d35fe1e39970ef86aabf8
Mei Ariel Ji Yazi Eight Drug Abuse Test Kits
TW: 美艾利爾 揣耶濟 八類藥物濫用檢測套組
Taiwan·Risk Class 2·ALERE SAN DIEGO, INC.·Registered Mar 21, 2006 – Mar 21, 2021CancelledRegistration details
- Analysis ID
- 5b5868963c0d35fe1e39970ef86aabf8
- Customs Code
- DHA00601617900
Company information
- Manufacturer
- ALERE SAN DIEGO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
Product details
- Intended Use
- Urine is qualitatively detected for amphetamines, barbiturates, benzodiazepines, cocaine, methadone, opium, tetrahydrocanabinol and their metabolites, and the presence of tricyclic antidepressants at specific cut-off values.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3100 Anandamide Test System
- Import Information
- import
Dates and status
- Registration Date
- Mar 21, 2006
- Expiry Date
- Mar 21, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Mei Ariel Ji Yazi Eight Drug Abuse Test Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5b5868963c0d35fe1e39970ef86aabf8 and manufactured by ALERE SAN DIEGO, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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