8 results · 22ms · Sources: EU EUDAMED, US FDA

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smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908. For use during orthopedic surgery.

FDA Enforcement
Class II ·Terminated·Smith & Nephew Orthopaedics Ltd. (Aurora)·August 18, 2021

Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR, REF Numbers: 74120246 (46 MM), 74122248 (48 MM), 74120250 (50 MM), 74122252 (52 MM), 74120254 (54 MM) Product Usage: Hip joint prosthesis

FDA Enforcement
Class II ·Terminated·Smith & Nephew, Inc.·September 16, 2015

Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD, STERILE R, Rx only, REF Numbers: 74121138 (38 MM), 74123140 (40 MM), 74121142 (42 MM), 74123144 (44 MM), 74121146 (46 MM). Product Usage: Hip joint prosthesis

FDA Enforcement
Class II ·Terminated·Smith & Nephew, Inc.·September 16, 2015

Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR, REF Numbers: 74120144 (44 MM), 74120146 (46 MM), 74122146 (46 MM), 74122148 (48 MM), 74120148 (48 MM), 74120150 (50 MM), 74122150 (50 MM), 74122152 (52 MM), 74120152 (52 MM), 74120154 (54 MM) Product Usage: Hip joint prosthesis

FDA Enforcement
Class II ·Terminated·Smith & Nephew, Inc.·September 16, 2015

SIMVIEW NT and SIMVIEW NT with IDI: October 01, 2012 Siemens ceased Simview distribution. Manufactured by: Mecaserto now known as Mecasim Parc de lEsplanade 9,Rue Niels Bohr 77400 Saint Thibault des Vignes- France The intended use of the SIEMENS branded SIMVIEW NT and SIMVIEW NT with IDI is a radiation therapy simulation system.

FDA Enforcement
Class II ·Terminated·Siemens Medical Solutions USA, Inc·January 29, 2014

BrightView X are gamma cameras; Designed for single or dual detector nuclear imaging.

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·March 9, 2016

BrightView XCT & BrightView XCT Upgrade, gamma cameras; For Single Proton Emission Computed Tomography.

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·March 9, 2016

BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·March 9, 2016