Taiwan FDA registration 6a4379f44b5dc413a7b0ca77fb567e34

"Quidel" Lyra Direct C. difficile Assay Rapid DNA Stool Sample Prep Kit (Non-Sterile)

TW: "快得利" 快速糞便樣本製備套組 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·QUIDEL CORPORATION·Registered Apr 13, 2015 – Apr 13, 2020Cancelled
Registration details
Analysis ID
6a4379f44b5dc413a7b0ca77fb567e34
License Form
Ministry of Health Medical Device Import No. 015096
Customs Code
DHA09401509604
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)
C2900 Microbial sample collection and delivery device
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 13, 2015
Expiry Date
Apr 13, 2020
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 Rapid DNA Stool Sample Prep Kit (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 6a4379f44b5dc413a7b0ca77fb567e34 and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is BIO-CHECK LABORATORIES 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.

Free DatabasePowered by Pure Global AI89,000+ Devices