31 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
The Micro Screw System, Micro Screw System Basic
FDA 510(k)
FDA Class 2
·Dental
Pantheon System
FDA UDI
ADLER ORTHO SPA·08050880238422·Pantheon Bridging Collar Ø 36 mm for Stem Ø 11 mm
OsteoMed
FDA UDI
Provision·B504OM32012100·
NeoFuse HA Enhanced PLIF/TLIF
FDA UDI
XENIX MEDICAL LLC·00818345020429·HA CAGE 20L x 12W x 10H
OsteoMed
FDA UDI
OSTEOMED LLC·00845694019484·1.0mm Drill, Manual
Responsive Respiratory, Inc.
FDA UDI
RESPONSIVE RESPIRATORY, INC.·00851440007322·Oxygen Regulator, 25 LPM CGA 870 w/ DISS & Barb
Prehma
FDA UDI
Keystone Industries·H66812012101·PREHMA SURGICAL ASPIRATOR 1/16 ( BAG X 25)
Viceroy
FDA UDI
DIOMEDICAL CO.,LTD.·08800113905122·VICEROY Rod - 6.0 (D)6x(L)210mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694073141·HPS 1.0mm Drill, Manual Sterile Qty 2
ARTERIA OCCLUSION BALLOON
FDA 510(k)
FDA Class 2
·Cardiovascular
HI-RES 9000 PHASED ARRAY CAROTID COIL
FDA 510(k)
FDA Class 2
·Radiology
BD PHASEAL¿ SPIKE CONNECTOR (C180J)
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·December 21, 2022
COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·July 29, 2011
URS Ø6 L40
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HWC·July 2, 2013
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·January 20, 2023
BD PHASEAL¿ SPIKE CONNECTOR
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·November 16, 2022
HANDPIECE MICS
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code OLO·January 26, 2017
BD PHASEAL¿ SPIKE CONNECTOR
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·October 15, 2022
BD PHASEAL¿ SPIKE CONNECTOR (C180J)
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FPA·October 13, 2022