Taiwan FDA registration 62042764cee27f5cee28893a4166df79
Bell Opium Test Reagent
TW: 貝爾鴉片檢驗試劑
Registration details
- Analysis ID
- 62042764cee27f5cee28893a4166df79
- Customs Code
- DHA00601627509
Company information
- Manufacturer
- SYNTRON BIORESEARCH INC.,
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Bell Pharmaceutical Co., Ltd
Product details
- Intended Use
- Rapid and qualitative competitive immunoassay was used to measure the presence or absence of opium and its proxy in urine when it was above 300ng/ml.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3650 Opium testing system
- Import Information
- import
Dates and status
- Registration Date
- Mar 30, 2006
- Expiry Date
- Mar 30, 2011
- Cancellation Date
- Nov 02, 2006
Cancellation information
- Status
- Logged out
- Reason
- 註銷藥商許可執照
About this record
Access comprehensive regulatory information for Bell Opium Test Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 62042764cee27f5cee28893a4166df79 and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Taiwan Bell Pharmaceutical Co., Ltd.
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.
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