Taiwan FDA registration 82ba10f7c6afde002975830041242ca8
"Quidel" AmpliVue C. difficile Assay (Non-Sterile)
TW: "快得利" 困難梭狀芽孢桿菌分子檢測套組 (未滅菌)
Taiwan·Risk Class 1·MD·QUIDEL CORPORATION·Registered Mar 09, 2015 – Mar 09, 2020CancelledRegistration details
- Analysis ID
- 82ba10f7c6afde002975830041242ca8
- License Form
- Ministry of Health Medical Device Import No. 014983
- Customs Code
- DHA09401498300
Company information
- Manufacturer
- QUIDEL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BIO-CHECK LABORATORIES LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2660 Microbial identification and assay equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 09, 2015
- Expiry Date
- Mar 09, 2020
- Cancellation Date
- May 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Quidel" AmpliVue C. difficile Assay (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 82ba10f7c6afde002975830041242ca8 and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is BIO-CHECK LABORATORIES LTD..
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