73 results
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28ms
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Sources: EU EUDAMED, US FDA
FLEXITOUCH SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Integra® Spider™ Limted Wrist Fusion System
FDA UDI
Ascension Orthopedics, Inc.·10381780064732·The Integra Spider Limited Wrist Fusion titaniu...
Spider Limited Wrist Fusion System
FDA UDI
Smith & Nephew, Inc.·00885556834725·SPIDER TITANIUM 2.8/18MM BONE SCREW
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037312810·STD TRIAL CUP FOR BOACH Ø32+18
Sterilance Press2 Pressure Activated Safety Lancet
FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630109925·Sterilance Press2 Pressure Activated Safety Lan...
Sterilance Press2 Safety Lancet 28G 1.8mm
FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630123112·
Sterilance Press2 Pressure Activated Safety Lancet
FDA UDI
SteriLance Medical (Suzhou) Inc.·16945630109147·Sterilance Press2 Pressure Activated Safety Lan...
Sterilance Press2 Disposable Safety Lancet
FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630115070·
Sterilance Press2 Pressure Activated Safety Lancet
FDA UDI
SteriLance Medical (Suzhou) Inc.·16945630109154·Sterilance Press2 Pressure Activated Safety Lan...
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037317471·STANDARD TRIAL FIXED CUP FOR BROACH Ø32 +18
NIRTRILE PATIENT EXAMINATION GLOVE (BLUE COLOR) POWDERED, NON STERILE
FDA 510(k)
FDA Class 1
·General Hospital
HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED SINGLE HELIX
FDA 510(k)
FDA Class 2
·Orthopedic
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·April 11, 2013
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·March 25, 2011
LIFEVEST WCD 3000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·June 18, 2008
GLIDESHEATH
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DYB·August 7, 2019
GLIDESHEATH
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DYB·July 7, 2022
GLIDESHEATH
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DYB·December 1, 2020
RADIFOCUS INTRODUCER
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DYB·May 19, 2022
RADIFOCUS INTRODUCER
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DYB·January 21, 2022