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Surelift Anchorsure - Anchor, soft-tissue implanted, non-biodegradable - ARTG 460867

Access comprehensive regulatory information for Surelift Anchorsure - Anchor, soft-tissue implanted, non-biodegradable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 460867 and sponsored by Innovative Medcare Technology Pty Ltd, manufactured by Desarrollo E Investigation Medica Aragonesa SL in Spain. The device registration started on August 27, 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.

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Class IIb
ARTG 460867
Class IIb
Surelift Anchorsure - Anchor, soft-tissue implanted, non-biodegradable
ARTG ID: 460867
Good Name: Innovative Medcare Technology Pty Ltd - Surelift Anchorsure - Anchor, soft-tissue implanted, non-biodegradable
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Intended Purpose

Surelift Anchorsure is used for attaching sutures to the sacropinous ligament for vaginal prolapse repair. It is a sacrospinous-ligament (SSL) fixation system for pelvic organ prolapse treatment. It consists of an anchor which is secured to the SSL using a specially designed applicator (Anchoring Handle), and an attached monofilament suture. The Anchor is made of PEEK and Suture made of PVDF.

Device Classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
460867
Start Date
August 27, 2024
Effective Date
August 27, 2024
Manufacturer
Country
Spain
Address
Pol Ind Mediavega Parcela 2 8, Calatayud, Zaragoza, 50300