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Instrument/analyser IVDs

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 R-Biopharm Pty Ltd, manufactured by SSI Diagnostica A/S in Denmark. The device registration started on November 26, 2020.

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
Class I
Instrument/analyser IVDs
Australia TGA ARTG Registered Device
Good Name: R-Biopharm Pty Ltd - Instrument/analyser IVDs
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Intended Purpose

Manual, semi-automated or automated equipment or apparatus that are intended for the processing, examining and/or providing information about a clinical specimen.

Device Classification
Risk Class
Class I
Product Type
IVD
ARTG Category
IVD
Registration Information
Start Date
November 26, 2020
Effective Date
November 26, 2020
Manufacturer
Country
Denmark
Address
Herredsvejen 2, Hillerod, 3400