Australia TGA ARTG record

Bone marrow biopsy needle, single-use

Australia TGA ARTG Registered Device · Pureplay Orthopaedics · Ranfac Corporation · Class IIa · Started August 04, 2022

Good Name: Pureplay Orthopaedics - Bone marrow biopsy needle, single-use

Device classification

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

Registration information

Start Date: August 04, 2022
Effective Date: August 04, 2022

Sponsor

Name: Pureplay Orthopaedics

Manufacturer

Name: Ranfac Corporation
Country: United States of America
Address: 30 Doherty Avenue, AVON, MA, 02322

Intended purpose

Biopsy Needle used for bone marrow aspiration. Single use

About this record

Access comprehensive regulatory information for Bone marrow biopsy needle, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Pureplay Orthopaedics, manufactured by Ranfac Corporation in United States of America. The device registration started on August 04, 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.