213 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STRYKER IRRIGATION TUBE SET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SW
FDA UDI
SW SAFETY SOLUTIONS INC.·00616489004035·PowerChem Neoprene Exam Gloves, Medium
PowerPICC
FDA UDI
Bard Access Systems, Inc.·00801741100222·Catheter Placement Kit
TEWA
FDA UDI
asia-med GmbH·04251282511203·TeWa CJ-Type 2275(s) Safe-T Sleeve: uncoated a...
TEWA
FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282503888·TeWa CJ-Type 2275(s) Safe-T Sleeve: uncoated a...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450155424·
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700004930·
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S1700004930·
BARCO MGD 221 2 MEGAPIXEL DIAGNOSTIC DISPLAY
FDA 510(k)
FDA Class 2
·Radiology
NOVA CORDLESS CURING LIGHT
FDA 510(k)
FDA Class 2
·Dental
THRUWAY GUIDE WIRE
FDA Adverse Event
Malfunction
·LAKE REGION MEDICAL·Product code DQX·March 12, 2013
CONTOUR
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·January 31, 2011
*
FDA Adverse Event
Malfunction
·GAMBRO DASCO S.P.A., MONITOR DIVISION·Product code FII·January 22, 2008
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 11, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·May 18, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·May 18, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code NKB·June 18, 2010
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·May 18, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·December 17, 2010