Taiwan FDA registration d081393705c2943abd92683caa025eca
Qui-visual chorionic gonadotropin assay reagent
TW: 奎可視絨毛膜促性腺激素測定試劑
Taiwan·Risk Class 2·QUIDEL CORPORATION·Registered Oct 22, 2008 – Oct 22, 2013CancelledRegistration details
- Analysis ID
- d081393705c2943abd92683caa025eca
- Customs Code
- DHA00601946401
Company information
- Manufacturer
- QUIDEL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BIOMERIEUX CHINA LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- Antibody antigen enzyme immune response to test human chorionic gonadotropin in serum or urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- import
Dates and status
- Registration Date
- Oct 22, 2008
- Expiry Date
- Oct 22, 2013
- Cancellation Date
- Aug 13, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Qui-visual chorionic gonadotropin assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d081393705c2943abd92683caa025eca and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is BIOMERIEUX CHINA LIMITED, TAIWAN BRANCH (HONG KONG).
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