14 results
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34ms
·
Sources: EU EUDAMED, US FDA
ELECTRONYSTAGMOGRAPH (ENG RECORDER)
FDA 510(k)
FDA Class 2
·Neurology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192589·Distal Reamer 18mm (Zimmer)
Lateral Perineal Post Mount Bracket
FDA UDI
MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430106408·
HALYARD
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918158242·ATC_LIFT SHEET_ARM BOARD COVER_Bags_Non sterile...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955930461·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955931567·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955932663·Percutaneous Transluminal Angioplasty Balloon C...
EXPA-SYL
FDA 510(k)
FDA Unclassified
·Unknown
InTone
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NIM-ECLIPSE® CONTROLLER
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code GWF·December 9, 2014
UNKNOWN_SPINE_PRODUCT
FDA Adverse Event
Injury
·STRYKER SPINE-FRANCE·Product code OVE·June 5, 2014
SIDEWINDER BLADE ICW
FDA Adverse Event
Malfunction
·ARTHROCARE CORPORATION·Product code GEI·November 21, 2012
BD L-CATH PICC AND BD SPLITTABLE NEEDLE INTRODUCER
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY·Product code LJS·September 22, 2010
Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.
FDA Enforcement
Class II
·Terminated·STERILMED, INC.·December 16, 2015