11 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MITOCHONDRIA EIA TEST KIT
FDA 510(k)
FDA Class 2
·Immunology
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780415145·Integra® Miltex® Tissue Nipper, 5", Convex Jaws
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074052311·SPREADER 2940251 CAM 7MM
VARIAX
FDA UDI
Stryker GmbH·07613327125641·Reduction Instrument Insert 2
Arthrex®
FDA UDI
ARTHREX, INC.·00888867524149·ECLIPSE SIZING PLATE, 51
GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587
FDA 510(k)
FDA Class 2
·Radiology
UNIVERSAL DIGITAL INTERFACE 2, UDI 2
FDA 510(k)
FDA Class 2
·Radiology
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·February 2, 2013
COATED VICRYL SUTURE
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAM·December 9, 2010
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 17, 2014
GE Healthcare, CARESCAPE Monitor B850, B650 or B450. Patient Monitor.
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·July 30, 2014