1. MicroPort Orthopedics’ patient information leaflets are created to provide information about your implant and are available here in an electronic format. A web browser with a PDF viewer is required to access all translations of the leaflet provided on this page.
  2. In order to select the correct implant leaflet, please refer to the back of the patient implant card provided to you by your HCP after surgery and look for the name of the device next to the MD symbol ( ).
  3. If you have lost your implant card or it is damaged, please follow the instructions below for “Implant card replacement”
  4. Based on the name of device implanted, select the appropriate link below. For example: Patient Leaflet for hip implants are located under “Hip Implant”
  5. Select the desired translation.

Printed translations of Patient Information Leaflets can be requested by calling MicroPort Orthopedics Customer Service at

Europe: +44.1244.572120

United States: 866.872.0211

Printed translations are provided free of charge to the requester within seven (7) days of request.

 

Hip Implants
Patient Leaflet for MicroPort Hip Systems (Australia) 159255-0
Patient Leaflet for PROCOTYL® P Acetabular System (EU) 159456-0
Patient Leaflet for PROFEMUR® Gladiator Classic stems (EU) 159319-0
Patient Leaflet for PROFEMUR® Z Revision and Z Classic stems (EU) 159253-0
Summary of Safety and Clinical Performance (SSCP) for PROCOTYL® P Acetabular System (EU) 02269
Summary of Safety and Clinical Performance (SSCP) for PROFEMUR® Gladiator Classic stems (EU) 02457
Summary of Safety and Clinical Performance (SSCP) for PROFEMUR® Z Revision and Z Classic stems (EU) 01770
Knee Implants
Patient Leaflet for EVOLUTION BIOFOAM TIBIAL BASE SCREWLESS (EU) 159229-0
Patient Leaflet for EVOLUTION® Revision Knee System (EU) 159247-0
Patient Leaflet for EVOLUTION® Stemmed CS Femur (Australia) 159648-0
Patient Leaflet for MicroPort Knee Systems (Australia) 159256-1
Summary of Safety and Clinical Performance (SSCP) for EVOLUTION BIOFOAM TIBIAL BASE SCREWLESS (EU) 01709
Summary of Safety and Clinical Performance (SSCP) for EVOLUTION® NitrX Knee System (EU) 02352
Summary of Safety and Clinical Performance (SSCP) for EVOLUTION® Revision Knee System (EU) 01989

 

CAUTION: The most recent revision of each patient information leaflet contains the most up-to-date information and is the only revision that is appropriate for device use. Previous revisions of patient information leaflets include obsolete information and should only be used as reference. To view previous revisions of patient information leaflets, please click here

 

IMPLANT CARD REPLACEMENT

In the event you need a replacement implant card, please click here