22 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HU-FRIEDY DENTAL CARTRIDGE SYRINGE
FDA 510(k)
FDA Class 2
·Dental
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450160756·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450160473·
KING SEPTEMS
FDA Adverse Event
Malfunction
·KING SEPTEMS·Product code LMA·November 1, 2012
MANUKAHD, MANUKAHD ROPE, MANUKAHD BORDER
FDA 510(k)
FDA Unclassified
·Unknown
DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973295·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970690·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970676·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970645·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970621·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970638·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970683·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970652·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970669·
RESTORE SENSOR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 20, 2013
INTRATHECAL CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·September 19, 2014
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 10, 2011
Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;
FDA Enforcement
Class II
·Terminated·Zimmer CAS·June 10, 2015
KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 4 / Adult Silicone King LAD¿ Patient Size: 50-70kg
FDA Enforcement
Class II
·Terminated·King Systems Corp.·November 28, 2012