34 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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APTUS ULNA SHORTENING 2.5
FDA 510(k)
FDA Class 2
·Orthopedic
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868558665·
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304010116·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868247958·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T1412320·14mm TLIF Implant 12mm Wide 32mm Length
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T14123270·14mm TLIF Implant 12mm Wide 32mm Length 7 degrees
ZEVO ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWQ·October 23, 2019
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973851·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970904·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970898·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973141·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973318·
ZEVO ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWQ·December 19, 2018
GETTIG UNIVERSAL VIAL ACCESS PIN
FDA 510(k)
FDA Class 2
·General Hospital
JOINSOON ELECTRONICS MFG CO. LTD HIGH SPEED DIGITAL THERMOMETER, MODEL TC-001
FDA 510(k)
FDA Class 2
·General Hospital
BD SAFETYGLIDE¿ NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·October 10, 2023
BD SAFETYGLIDE¿ NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·October 10, 2023
INCORPORATE
FDA UDI
SPINAL ELEMENTS·00840606151726·14 X 12 CERVICAL TRIALS 32MM 10° LORDOSIS
INCORPORATE
FDA UDI
SPINAL ELEMENTS·00840606151535·14 X 12 CERVICAL TRIALS 32MM 0° LORDOSIS
FREESTYLE LITE
FDA Adverse Event
Malfunction
·Product code NBW·October 3, 2014