Taiwan FDA registration f14f61e8eb9f61bbb164bbf368911167

"Firui" pneumonia detection quality control kit (unsterilized)

TW: "菲瑞" 肺炎檢測品管套組(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Maine Molecular Quality Controls, Inc.·Registered Mar 11, 2020 – Mar 11, 2030Active
Registration details
Analysis ID
f14f61e8eb9f61bbb164bbf368911167
Customs Code
DHA09402135300
Company information
Manufacturer Country
United States
Authorized Representative
MEDTRI CO., LTD.
Product details
Intended Use
Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1660 Quality control materials (analytical and non-analytical)
Import Information
import
Dates and status
Registration Date
Mar 11, 2020
Expiry Date
Mar 11, 2030
About this record

Access comprehensive regulatory information for "Firui" pneumonia detection quality control kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f14f61e8eb9f61bbb164bbf368911167 and manufactured by Maine Molecular Quality Controls, Inc.. The authorized representative in Taiwan is MEDTRI CO., 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