ARTG 467285Guidewire SFC-400/6-018/Niti-Pt 400 cm, 0.018'' - Catheter guide wire
ARTG ID: 467285 · Cryolife Medical (Australia) Company Pty Ltd · EPflex Feinwerktechnik GmbH · Class III · Started November 05, 2024
Good Name: Cryolife Medical (Australia) Company Pty Ltd - Guidewire SFC-400/6-018/Niti-Pt 400 cm, 0.018'' - Catheter guide wire
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 467285
- Start Date
- November 05, 2024
- Effective Date
- November 05, 2024
- Country
- Germany
- Address
- Im Schwollbogen 24, Dettingen Erms, D-72581
Guide wires are intended to be placed in the human body invasively or surgically-invasively through a natural or artificially produced body orifice or minimally-invasively through a port in the blood vessels of the central circulatory system, to be guided by controllable distal and proximal ends to a certain area of the human body to be used as a guide for catheters or other medical devices which are intended to be used in this area of the body.
Access comprehensive regulatory information for Guidewire SFC-400/6-018/Niti-Pt 400 cm, 0.018'' - Catheter guide wire in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 467285 and sponsored by Cryolife Medical (Australia) Company Pty Ltd, manufactured by EPflex Feinwerktechnik GmbH in Germany. The device registration started on November 05, 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.