Australia TGA ARTG record

Instrument/analyser IVDs

Australia TGA ARTG Registered Device · Revvity Pty Ltd · Revvity Health Sciences Inc · Class I · Started February 13, 2024

Good Name: Revvity Pty Ltd - Instrument/analyser IVDs

Device classification

Risk Class: Class I
Product Type: IVD
ARTG Category: IVD

Registration information

Start Date: February 13, 2024
Effective Date: June 20, 2024

Sponsor

Name: Revvity Pty Ltd

Manufacturer

Name: Revvity Health Sciences Inc
Country: United States of America
Address: 68 Elm Street, Hopkinton, MA, 01748

Intended purpose

Manual, semi-automated or automated equipments or apparatus that are intended by the manufacturer to be used as an in vitro diagnostic medical device (IVD) for the purposes of processing, examining and/or providing information about a clinical specimen.

About this record

Access comprehensive regulatory information for Instrument/analyser IVDs in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Revvity Pty Ltd, manufactured by Revvity Health Sciences Inc in United States of America. The device registration started on February 13, 2024.

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.