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Comprehensive Posterior System - Bone-screw internal spinal fixation system, sterile

Access comprehensive regulatory information for Comprehensive Posterior System - Bone-screw internal spinal fixation system, sterile in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Emergo Asia Pacific Pty Ltd T/a Emergo Australia, manufactured by Ulrich GmbH & Co KG in Germany. The device registration started on February 27, 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.

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Class IIb
Class IIb
Comprehensive Posterior System - Bone-screw internal spinal fixation system, sterile
Australia TGA ARTG Registered Device
Good Name: Emergo Asia Pacific Pty Ltd T/a Emergo Australia - Comprehensive Posterior System - Bone-screw internal spinal fixation system, sterile
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Intended Purpose

System, intended to be used for fixation, stabilisation or correction of spinal segments in thoracic, lumbar or sacral spine or illium.

Device Classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
February 27, 2024
Effective Date
February 27, 2024
Manufacturer
Country
Germany
Address
Buchbrunnenweg 12, Ulm, 89081