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MICRORAPTOR Knotless REGENESORB Suture Anchor - Fixation anchor, soft-tissue, biodegradable - ARTG 368071

Access comprehensive regulatory information for MICRORAPTOR Knotless REGENESORB Suture Anchor - Fixation anchor, soft-tissue, biodegradable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 368071 and sponsored by Smith & Nephew Pty Ltd, manufactured by Smith & Nephew Inc Endoscopy Division in United States of America. The device registration started on June 03, 2021.

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 III
ARTG 368071
Class III
MICRORAPTOR Knotless REGENESORB Suture Anchor - Fixation anchor, soft-tissue, biodegradable
ARTG ID: 368071
Good Name: Smith & Nephew Pty Ltd - MICRORAPTOR Knotless REGENESORB Suture Anchor - Fixation anchor, soft-tissue, biodegradable
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Intended Purpose

The Smith+Nephew MICRORAPTOR Knotless REGENESORB Suture Anchor is intended for the reattachment of soft tissue to bone for the following indications: Hip: Acetabular labrum repair/reconstruction; Shoulder: Capsular stabilization, Bankart repair, Anterior shoulder instability, SLAP lesion repairs, Capsular shift or capsulolabral reconstructions; Biceps tenodesis.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
368071
Start Date
June 03, 2021
Effective Date
June 03, 2021
Manufacturer
Country
United States of America
Address
150 Minuteman Road, ANDOVER, MA, 01810-1031