For patient information leaflets please refer to your implant’s name below

Home > A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Index

BI-MENTUM Cemented Cup

BI-MENTUM Revision Cup

BI-MENTUM PE Liner

BI-MENTUM Plus Cup

BI-MENTUM Pressfit Cup

BRAVO FLOW DIVERTER

EIT Cellular Titanium® ALIF Cage

EIT Cellular Titanium® Cervical Cage

EIT Cellular Titanium® LLIF Cage

EIT Cellular Titanium® PLIF Cage

EIT Cellular Titanium® TLIF Cage

GYNECARE TVT

Healix Advance BR Anchor with Dynacord Suture

Healix Advance Knotless BR Anchor

Healix Advance Knotless PEEK Anchor

Mentor Textured and Smooth Gel Breast Implants

Mentor Smooth Saline Breast Implants

Mentor CPX4 Textured Breast Tissue Expanders

PROCEED Surgical Mesh

SmartMix Cemvac


Please be advised that not all Patient Information Leaflets (PILs) are currently available on the Johnson & Johnson Medical website, as it is currently under development.

Reporting adverse effects

If you wish to report any adverse effects you believe are a result of your implanted medical device, please talk with your surgeon or report the information to Johnson & Johnson Medical Product Safety Department on:

Email: [email protected]

Reports may also be made directly to the Therapeutic Goods Administration via the website

http://www.tga.gov.au/reporting-problems

Or 

If you are based in New Zealand, Medsafe via the website

https://www.medsafe.govt.nz/regulatory/DevicesNew/9AdverseEvent.asp

Australia Sponsor
Johnson & Johnson Medical Pty Ltd
1 - 5 Khartoum Road NORTH RYDE, NSW 2113 Tel: (1300 562 711)

New Zealand Sponsor:
Johnson & Johnson Medical New Zealand Ltd
Division of Johnson & Johnson (NZ) Ltd, PO Box 62185, Mt Wellington, Auckland, New Zealand