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Side-notch biopsy gun, single-use

Access comprehensive regulatory information for Side-notch biopsy gun, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Ultramed, manufactured by Zhejiang CuraWay Medical Technology Co Ltd in China. The device registration started on October 08, 2021.

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 IIa
Class IIa
Side-notch biopsy gun, single-use
Australia TGA ARTG Registered Device
Good Name: Ultramed - Side-notch biopsy gun, single-use
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Intended Purpose

A hand-operated, non-electronic, surgical instrument designed for the automatic extraction of a small tissue sample from an anatomical structure (a biopsy), while causing minimal surrounding tissue damage, for tissue pathological examination/test. It consists of both: 1) a handpiece with a spring-loaded mechanism and release trigger; and 2) a percutaneous, distal, needle-like portion with a side-notch cutter which when activated causes a sharp, sliding cannula to slice a segment of tissue. It is typically used to obtain samples of soft tissue from the kidneys, prostate, pancreas, liver, and breast, often performed under image guidance. This is a single-use device.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
October 08, 2021
Effective Date
October 08, 2021
Sponsor
Manufacturer
Country
China
Address
Room 106 Building 1 #600 21st Street Economic & Technology Development Area, Hangzhou, Zhejiang, 310018