Pure Global

Probe, <specify> - ARTG 233695

Access comprehensive regulatory information for Probe, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 233695 and sponsored by Lateral Medical, manufactured by Cheetah Medical Israel Ltd in Israel. The device registration started on February 12, 2015.

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.

Free Database
Powered by Pure Global AI
TGA ARTG Official Data
Class I
ARTG 233695
Class I
Probe, <specify>
ARTG ID: 233695
Good Name: Lateral Medical - Probe, <specify>
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Intended Purpose

The sensors are attached to the monitoring device which calculates Heamodynamic readings.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
233695
Start Date
February 12, 2015
Effective Date
February 12, 2015
Sponsor
Manufacturer
Country
Israel
Address
38 Habarzel Street, Tel Aviv, 69710