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Surgical procedure kit, general-purpose, reusable - ARTG 396784

Access comprehensive regulatory information for Surgical procedure kit, general-purpose, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 396784 and sponsored by Life Healthcare Pty Ltd, manufactured by Trimed Inc in United States of America. The device registration started on September 30, 2022.

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
ARTG 396784
Class I
Surgical procedure kit, general-purpose, reusable
ARTG ID: 396784
Good Name: Life Healthcare Pty Ltd - Surgical procedure kit, general-purpose, reusable
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Intended Purpose

TriMedยฎ Reusable Surgical Instruments are an array of generic and device-specific instruments designed specifically for orthopedic surgery. Such tools facilitate orthopedic surgeons to achieve, enable or expedite specific tasks related to surgical techniques and implant systems. TriMed Reusable Surgical Instruments perform, but are not limited to, the following functions: fastening, bending, crimping, impacting, inserting/extracting/retracting, grasping, repositioning, aligning/aiming, trial/templating, tensioning, torqueing, cutting, clamping, and elevating. TriMed Reusable Surgical Instruments are devices which are not connected to electrically powered equipment for use. TriMed surgical instruments and implants are supplied to the user in a system-dedicated, non-sterile rigid instrument tray that accommodates the specific TriMed devices to be processed for inspection, cleaning, sterilization, transportation and storage.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
396784
Start Date
September 30, 2022
Effective Date
September 30, 2022
Manufacturer
Country
United States of America
Address
27533 Avenue Hopkins, Santa Clarita, CA, 91355