Taiwan FDA registration d997b03bc523c255e90d96fe9ad4b0d4

"Fishery" Gastrointestinal Pathogen Multi-label Nucleic Acid Detection Quality Tube Set (Unwiped Bacteria)

TW: "菲瑞" 胃腸道病原體多標的核酸檢測品管套組(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Maine Molecular Quality Controls, Inc.·Registered Oct 07, 2024 – Oct 07, 2029Active
Registration details
Analysis ID
d997b03bc523c255e90d96fe9ad4b0d4
Customs Code
DHA09402362106
Company information
Manufacturer Country
United States
Authorized Representative
MEDTRI CO., LTD.
Product details
Intended Use
It is limited to the scope of the first class of the medical equipment classification and classification management method "Quality Control Materials (Analytical and Non-Analytical) (A.1660)".
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
Oct 07, 2024
Expiry Date
Oct 07, 2029
About this record

Access comprehensive regulatory information for "Fishery" Gastrointestinal Pathogen Multi-label Nucleic Acid Detection Quality Tube Set (Unwiped Bacteria) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d997b03bc523c255e90d96fe9ad4b0d4 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