ARTG 370316Choice 380 Silver / Copper, 7 MED - Intrauterine device, metal-covered
ARTG ID: 370316 · Contiform International Pty Ltd · Laboratoire 7 MED · Class III · Started June 28, 2021
Good Name: Contiform International Pty Ltd - Choice 380 Silver / Copper, 7 MED - Intrauterine device, metal-covered
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 370316
- Start Date
- June 28, 2021
- Effective Date
- June 28, 2021
- Country
- France
- Address
- Bioparc, Hauterive, 03270
The intrauterine Device Choice 380 Silver / Copper- 7MED NSTA(Standard model) and NSHA (Short model) are composed of two flexible arms made of polyethylene branching off of a vertical stem around which 380 square milimitres of copper is wound. The contraceptive activity of the device is mainly due to the presence of a foreign body in the intrauterine cavity. This action is reinforced in an ancillary manner by the presence of cooper. After oxidation, the copper atoms are distributed locally in the cervical mucus and endometrium, preventing fertilisation and rendering the endometrium unsuitable for implantation.
Access comprehensive regulatory information for Choice 380 Silver / Copper, 7 MED - Intrauterine device, metal-covered in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 370316 and sponsored by Contiform International Pty Ltd, manufactured by Laboratoire 7 MED in France. The device registration started on June 28, 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.