12 results
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19ms
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Sources: EU EUDAMED, US FDA
SELF-RETAINING SOFT TISSUE RETRACTOR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
BeneVision N Series Patient Monitors (Including BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19. BeneVision N22, BeneVision N1)
FDA 510(k)
FDA Class 2
·Cardiovascular
HANSEN MEDICAL DILATOR FOR ARTISAN CONTROL CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082278·Screw, polyaxial, Ø 7.5 mm, length 40 mm, not c...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082315·Screw, polyaxial, Ø 7.5 mm, length 60 mm, not c...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082308·Screw, polyaxial, Ø 7.5 mm, length 55 mm, not c...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082292·Screw, polyaxial, Ø 7.5 mm, length 50 mm, not c...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082285·Screw, polyaxial, Ø 7.5 mm, length 45 mm, not c...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082261·Screw, polyaxial, Ø 7.5 mm, length 35 mm, not c...
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·October 25, 2010
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·December 20, 2012
COGNIS
FDA Adverse Event
Death
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·June 18, 2014