ARTG 467885

Manual blood lancing device, single-use

ARTG ID: 467885 · Genesis Biotech Pty Ltd · Shandong Lianfa Medical Plastic Products Co Ltd · Class IIa · Started November 10, 2024

Good Name: Genesis Biotech Pty Ltd - Manual blood lancing device, single-use

Device classification

Risk Class: Class IIa
Product Type: Single Device Product
ARTG Category: General

Registration information

ARTG ID: 467885
Start Date: November 10, 2024
Effective Date: November 10, 2024

Sponsor

Name: Genesis Biotech Pty Ltd

Manufacturer

Name: Shandong Lianfa Medical Plastic Products Co Ltd
Country: China
Address: No 1 Shuangshan Sanjian Road, Zhangqiu City, Jinan Shandong, 250200

Intended purpose

Sterile contact activated safety lancet for obtaining a finger stick blood sample

About this record

Access comprehensive regulatory information for Manual blood lancing device, 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 467885 and sponsored by Genesis Biotech Pty Ltd, manufactured by Shandong Lianfa Medical Plastic Products Co Ltd in China. The device registration started on November 10, 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.