Taiwan FDA registration 50d55b503260293c9dea422dd8437b15
"Quidel" Sofia S.pneumoniae FIA (Non-Sterile)
TW: "會得" 舒妃雅肺炎鏈球菌快速螢光酵素免疫分析檢測套組 (未滅菌)
Taiwan·Risk Class 1·MD·QUIDEL CORPORATION·Registered Sep 26, 2016 – Sep 26, 2021CancelledRegistration details
- Analysis ID
- 50d55b503260293c9dea422dd8437b15
- License Form
- Ministry of Health Medical Device Import No. 017025
- Customs Code
- DHA09401702504
Company information
- Manufacturer
- QUIDEL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3740 Streptococcus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 26, 2016
- Expiry Date
- Sep 26, 2021
- Cancellation Date
- Aug 31, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Quidel" Sofia S.pneumoniae FIA (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 50d55b503260293c9dea422dd8437b15 and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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