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Specimen receptacle IVDs - ARTG 402226

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 402226 and sponsored by Sanofi-Aventis Australia Pty Ltd, manufactured by Eastern Business Forms Inc in United States of America. The device registration started on January 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 402226
Class I
Specimen receptacle IVDs
ARTG ID: 402226
Good Name: Sanofi-Aventis Australia Pty Ltd - Specimen receptacle IVDs
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Intended Purpose

Intended to collect specimens of a patient's blood and serve as a receptacle to contain and preserve the specimen in the form of a dried blood spot, as carried out by a healthcare professional, pending being transported to a laboratory for in vitro diagnosis examination.

Device Classification
Risk Class
Class I
Product Type
IVD
ARTG Category
IVD
Registration Information
ARTG ID
402226
Start Date
January 16, 2023
Effective Date
January 16, 2023
Manufacturer
Country
United States of America
Address
530 Old Sulphur Springs Road, Greenville, SC, 29607