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Surgical procedure kit, ophthalmic, non-medicated, single-use - ARTG 461889

Access comprehensive regulatory information for Surgical procedure kit, ophthalmic, non-medicated, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 461889 and sponsored by Defries Industries Pty Ltd, manufactured by GRI Medical & Electronic Technology Co Ltd in China. The device registration started on September 03, 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 IIa
ARTG 461889
Class IIa
Surgical procedure kit, ophthalmic, non-medicated, single-use
ARTG ID: 461889
Good Name: Defries Industries Pty Ltd - Surgical procedure kit, ophthalmic, non-medicated, single-use
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Intended Purpose

Ophthalmic packs are comprised of various sterile medical devices and products that the clinicians have determined are necessary to perform various types of ophthalmic procedures for all patients, regardless of age, ethnicity, and gender, as determined by the physician.

Device Classification
Risk Class
Class IIa
Product Type
Procedure Pack
ARTG Category
General
Registration Information
ARTG ID
461889
Start Date
September 03, 2024
Effective Date
September 03, 2024
Manufacturer
Country
China
Address
1805 Honggao Road, Jiaxing, Zhejiang, 314031