Taiwan FDA registration 7feea2cb3449fe6d4829c0107b7c02f1
“Quidel” Lyra Direct C. difficile Assay (Non-Sterile)
TW: “快得利”萊拉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 Dec 31, 2014 – Dec 31, 2019CancelledRegistration details
- Analysis ID
- 7feea2cb3449fe6d4829c0107b7c02f1
- License Form
- Ministry of Health Medical Device Import No. 014812
- Customs Code
- DHA09401481202
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
- Dec 31, 2014
- Expiry Date
- Dec 31, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Quidel” Lyra Direct 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 7feea2cb3449fe6d4829c0107b7c02f1 and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is BIO-CHECK LABORATORIES LTD..
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