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Anoscope, single-use - ARTG 482747

Access comprehensive regulatory information for Anoscope, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 482747 and sponsored by Medical Specialties Australasia Pty Ltd, manufactured by THD SpA in Italy. The device registration started on March 17, 2025.

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 482747
Class I
Anoscope, single-use
ARTG ID: 482747
Good Name: Medical Specialties Australasia Pty Ltd - Anoscope, single-use
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Intended Purpose

Intended for physician use during anoscopy procedures to examine the anal canal and the lower rectum and, when used in conjunction with additional accessories included in the kit (such as liquid dispenser, suction tubing), allows various diagnostic and therapeutic procedures to be performed.

Device Classification
Risk Class
Class I
Product Type
Procedure Pack
ARTG Category
General
Registration Information
ARTG ID
482747
Start Date
March 17, 2025
Effective Date
March 17, 2025
Manufacturer
Country
Italy
Address
Via per Carpi 15/B, Correggio RE, 42015