Product 11 consists of all product under product code JDI || , and same usage: || Item no: || 902602500 6 DEGREE COCR FEM HEAD 26 || 902602600 6 DEGREE COCR FEM HEAD 26 || 902602700 6 DEGREE COCR FEM HEAD 26 || 902602800 6 DEGREE COCR FEM HEAD 28 || 902602900 6 DEGREE COCR FEM HEAD 28 || 902603000 6 DEGREE COCR FEM HEAD 28 || 902603300 6 DEGREE COCR FEM HEAD 32 || 902603200 6 DEGREE COCR FEM HEAD 32 || Product Usage: || For use in total or hemi hip arthroplasty
“The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Brazil, Bolivia, Canada, Chile, China, Colombia, Ecuador, El Salvador, India, Japan, Malaysia, Mexico, Netherlands, New Zealand, Nicaragua, Panama, Seoul-Korea, Singapore, Taiwan, Thailand, and UAE.
Description du dispositif
PATELLO-FEMORAL JOINT SYSTEM GENDER SOLUTIONS PATELLO-FEMORAL¿ || Osteoarthritis, traumatic arthritis, polyarthritis, and/or severe chondrocalcinosis of the patellofemoral joint.
Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Brazil, Bolivia, Canada, Chile, China, Colombia, Ecuador, El Salvador, India, Japan, Malaysia, Mexico, Netherlands, New Zealand, Nicaragua, Panama, Seoul-Korea, Singapore, Taiwan, Thailand, and UAE.
Description du dispositif
ZIMMER PATELLA FEMORAL JOINT¿ || Osteoarthritis, traumatic arthritis, polyarthritis, and/or severe chondrocalcinosis of the patellofemoral joint.
Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Brazil, Bolivia, Canada, Chile, China, Colombia, Ecuador, El Salvador, India, Japan, Malaysia, Mexico, Netherlands, New Zealand, Nicaragua, Panama, Seoul-Korea, Singapore, Taiwan, Thailand, and UAE.
Description du dispositif
ZUK PRC FEM SZB RMED/LLAT¿ || ZUK PRC FEM SZC LMED/RLAT¿ || ZUK PRC FEM SZC RMED/LLAT¿ || NGU PRC FEM SZD LMED/RLAT¿ || ZUK PRC FEM SZD RMED/LLAT¿ || ZUK PRC FEM SZE LMED/RLAT || ZUK PRC FEM SZF RMED/LLAT || " These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or function. - Varus or valgus deformities. - Revision of previous arthroplasty procedures. " These devices are indicated for cemented use only. " The Zimmer Unicompartmental Knee System is designed for use when load bearing ROM is expected to be less than or equal to 155 degrees.