65 results
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58ms
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Sources: EU EUDAMED, US FDA
WILLO 32, INC.
FDA registration
WILLO 32, INC.·1 product·🇺🇸 United States
Willo
FDA UDI
Willo 32, Inc.·00860556002602·
Aquilion 32 CT System; Model number TSX-101 A/K The product is an x-ray device that uses digital geometry to generate a three-dimensional image of the inside of an object from a large series of two-dimensional X-ray images take around a single axis of rotation
FDA Recall
Terminated
·Toshiba American Medical Systems Inc·Product code JAK·January 8, 2009
Aquilion 32 CT System; Model number TSX-101 A/I The product is an x-ray device that uses digital geometry to generate a three-dimensional image of the inside of an object from a large series of two-dimensional X-ray images take around a single axis of rotation
FDA Recall
Terminated
·Toshiba American Medical Systems Inc·Product code JAK·January 8, 2009
Aquilion 32 CT System; Model number TSX-101 A/E The product is an x-ray device that uses digital geometry to generate a three-dimensional image of the inside of an object from a large series of two-dimensional X-ray images take around a single axis of rotation.
FDA Recall
Terminated
·Toshiba American Medical Systems Inc·Product code JAK·January 8, 2009
Biomet Vanguard Width Checker, Part Number: 32-487062, 67.5/75 Sizing Wing, Biomet Orthopedics, Inc., Warsaw, IN; The device is a preparatory instrument used for femoral knee insertion.
FDA Recall
Terminated
·Biomet, Inc.·Product code HWT·February 12, 2008
Aquilion 64 CT System; Model number TSX-101 A/J The product is an x-ray device that uses digital geometry to generate a three-dimensional image of the inside of an object from a large series of two-dimensional X-ray images take around a single axis of rotation
FDA Recall
Terminated
·Toshiba American Medical Systems Inc·Product code JAK·January 8, 2009
Aquilion 64 CT System; Model number TSX-101 A/D The product is an x-ray device that uses digital geometry to generate a three-dimensional image of the inside of an object from a large series of two-dimensional X-ray images take around a single axis of rotation
FDA Recall
Terminated
·Toshiba American Medical Systems Inc·Product code JAK·January 8, 2009
Aquilion 64 CT System; Model number TSX-101 A/H The product is an x-ray device that uses digital geometry to generate a three-dimensional image of the inside of an object from a large series of two-dimensional X-ray images take around a single axis of rotation
FDA Recall
Terminated
·Toshiba American Medical Systems Inc·Product code JAK·January 8, 2009
DURAMAX 15.5 F x 32 cm Chronic Hemodialysis Catheter Set (With Cuff 27 cm from Tip), DuraMax Stacked Tip 32 cm Str. Basic Kit, Catalog No./REF 10302805, STERILE --- AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804 USA The AngioDynamics DuraMax Chronic Hemodialysis Catheter is indicated for use in attaining long-term vascular access for Hemodialysis and apheresis.
FDA Recall
Terminated
·Angiodynamics, Inc.·Product code MSD·January 24, 2011
Atec Insignia Anterior Cervical Plate System, REF 136-0232 Insignia, ACP, 2-Level, 32 mm, Rx Only, Non-Sterile, UDI: (01)00190376268361
FDA Recall
Terminated
·Alphatec Spine, Inc. 1950 Camino Vida Roble·Product code KWQ·April 26, 2021
Angiodynamics DuraMax 15.5F x 32 cm Chronic Hemodialysis Catheter Set (with Cuff 27cm from Tip) --- Catalog No. [REF] 10302805 --- MANUFACTURED IN USA AngioDynamics, Inc., 603 Queensbury Avenue, Queensbury, NY USA 12804 Product Usage: indicated for use in attaining long-term vascular access for Hemodialysis and Apheresis.
FDA Recall
Terminated
·Angiodynamics Worldwide Headquarters·Product code MSD·December 30, 2011
Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system
FDA Recall
Open, Classified
·Orthoscan, Inc.·Product code OWB·August 8, 2024
Ziehm Solo. Digital Mobile C-arm
FDA Recall
Open, Classified
·Orthoscan, Inc.·Product code OWB·August 8, 2024
Ziehm Solo FD. Interventional fluoroscopic x-ray system
FDA Recall
Open, Classified
·Orthoscan, Inc.·Product code OWB·August 8, 2024
Ziehm Vision R. Iterventional fluoroscopic x-ray system
FDA Recall
Open, Classified
·Orthoscan, Inc.·Product code OWB·August 8, 2024
Ziehm Vision FD. Interventional fluoroscopic x-ray system
FDA Recall
Open, Classified
·Orthoscan, Inc.·Product code OWB·August 8, 2024
Ziehm Vision system, x-ray, tomography, computed.
FDA Recall
Open, Classified
·Orthoscan, Inc.·Product code JAK·August 8, 2024
Ziehm Vision RFD. Interventional fluoroscopic x-ray system
FDA Recall
Open, Classified
·Orthoscan, Inc.·Product code OWB·August 8, 2024
ViperWire Advance Peripheral Guide Wire, Sterilized with Ethylene Oxide, Rx Only. Part number 72023-02, Model Number VPR-GW-17. Five (5) guide wire pouches in one (1) guide wire box. For use with CSI Peripheral Orbital Atherectomy Devices (OAD), including Stealth 360 and Diamondback 360. Cardiovascular.
FDA Recall
Terminated
·Cardiovascular Systems Inc·Product code MCW·June 13, 2016