15 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100271·SAUER INFANT SPECULUM
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0153000·Guide, Drill Only, Double Barrel, Fixed
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955936609·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955938948·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955937774·Percutaneous Transluminal Angioplasty Balloon C...
MICROSURGICAL INSTRUMENTS
FDA 510(k)
FDA Class 2
·Orthopedic
PERMANENT PACING LEAD
FDA 510(k)
FDA Class 3
·Cardiovascular
POLARIS LOOP URETERAL STENT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code FAD·March 26, 2007
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·May 27, 2014
XENFORM SOFT TISSUE REPAIR MATRIX
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code PAJ·July 15, 2015
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·January 9, 2013
POLARIS LOOP URETERAL STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code FAD·March 26, 2007
POLARIS LOOP URETERAL STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code FAD·March 26, 2007
INTELLIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·March 10, 2021