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Punch, surgical, biopsy

Access comprehensive regulatory information for Punch, surgical, biopsy in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Ebos Group Australia Pty Ltd, manufactured by Paramount Surgimed Ltd in India. The device registration started on December 27, 2019.

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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Class IIa
Class IIa
Punch, surgical, biopsy
Australia TGA ARTG Registered Device
Good Name: Ebos Group Australia Pty Ltd - Punch, surgical, biopsy
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Intended Purpose

The device is used for obtaining full-thickness skin specimen. The device is invasive device and for transient use.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
December 27, 2019
Effective Date
December 27, 2019
Manufacturer
Country
India
Address
HO 1 LSC Okhla Industrial Area, Phase - II, New Delhi India, 110 020