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Specimen receptacle IVDs - ARTG 422531

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 422531 and sponsored by Revvity Pty Ltd, manufactured by Revvity Health Sciences Inc in United States of America. The device registration started on September 26, 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 422531
Class I
Specimen receptacle IVDs
ARTG ID: 422531
Good Name: Revvity Pty Ltd - Specimen receptacle IVDs
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Intended Purpose

RevvityTM 226 Sample Collection Device is intended to be used as a medium to collect and transport blood specimen spots to a laboratory. The sample is to be collected by qualified laboratory professionals.

Device Classification
Risk Class
Class I
Product Type
IVD
ARTG Category
IVD
Registration Information
ARTG ID
422531
Start Date
September 26, 2023
Effective Date
September 26, 2023
Sponsor
Manufacturer
Country
United States of America
Address
17 P & N Drive, Greenville, SC, 29611