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Specimen receptacle IVDs - ARTG 425682

Access comprehensive regulatory information for Specimen receptacle IVDs in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 425682 and sponsored by Roche Diagnostics Australia Pty Limited, manufactured by Foundation Medicine Inc in United States of America. The device registration started on October 16, 2023.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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TGA ARTG Official Data
Class I
ARTG 425682
Class I
Specimen receptacle IVDs
ARTG ID: 425682
Good Name: Roche Diagnostics Australia Pty Limited - Specimen receptacle IVDs
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Intended Purpose

The FoundationOneยฎLiquid CDx (F1LCDx) Specimen Collection Kit is intended to allow the collection and transport of whole blood, from the specimen collection site to the clinical laboratory, for the purpose of testing with the F1LCDx Assay. The cell-free DNA collection tube, included in the F1LCDx Specimen Collection Kit, is a direct draw whole blood collection tube intended for collection, stabilization, and transportation of whole blood specimens, and for the preservation of nucleated cells to enable analysis of cell-free DNA.

Device Classification
Risk Class
Class I
Product Type
IVD
ARTG Category
IVD
Registration Information
ARTG ID
425682
Start Date
October 16, 2023
Effective Date
October 16, 2023
Manufacturer
Country
United States of America
Address
150 Second Street, Cambridge, MA, 02141