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Soft-tissue anchor, non-bioabsorbable

Access comprehensive regulatory information for Soft-tissue anchor, non-bioabsorbable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Stryker Australia Pty Ltd, manufactured by Riverpoint Medical LLC in United States of America. The device registration started on March 23, 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 IIb
Class IIb
Soft-tissue anchor, non-bioabsorbable
Australia TGA ARTG Registered Device
Good Name: Stryker Australia Pty Ltd - Soft-tissue anchor, non-bioabsorbable
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Intended Purpose

Intended for use in the fixation of bone and soft tissue in orthopedic procedures.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
March 23, 2023
Effective Date
March 23, 2023
Manufacturer
Country
United States of America
Address
825 NE 25th Avenue, Portland, OR, 97232