23 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL
FDA 510(k)
FDA Class 2
·Radiology
Silicone Evacuator Kit
FDA UDI
C. R. Bard, Inc.·00801741050053·100cc Silicone Evacuator Kit, Medium 1/8" (10Fr...
REMEEX SYSTEM FOR URINARY INCONTINENCE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PVS BASIC 2; EPIC 2
FDA 510(k)
FDA Class 2
·Ophthalmic
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180502747·Curette, Teardrop, 15° Up Angled, Smooth, Size 2
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·February 21, 2011
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·November 30, 2011
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·January 16, 2012
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·January 6, 2011
FR CLERMONT FERRAND
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·October 3, 2012
MERCY HSP PITTSBURGH PA 1
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DWE·May 7, 2009
HCSG/HENDRICK MED/ABLNE TX 1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·February 16, 2010
DIDECO COMPACTFLO EVO
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·January 16, 2013
DIDECO COMPACTFLO EVO
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code KFM·December 13, 2012
DIDECO COMPACTFLO EVO
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·October 18, 2012
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 23, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 1, 2011
ISOFLEX S
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·July 11, 2008
EPD 60000 RPM
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HWE·June 27, 2017
DRILL BIT Ø1.8 F/MATMAND L125 2FLUTE F/0
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code DZI·September 3, 2013