11 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTERMEDICS ORTHOPEDICS SAW BLADE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Audit MicroControls Control FD Assayed Chemistry, Level 2
FDA UDI
AALTO SCIENTIFIC·B085K0312100·
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515240360·Jansen Middleton Sept Fcps, 4x11mm
ELECTRONIC THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
MODEL 4951M MYOCARDIAL UNIPOLAR LEAD
FDA 510(k)
FDA Class 3
·Cardiovascular
DRILL, AO, STERILE 4, 2X340 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 23, 2011
JUGGERKNOT 1.4MM SHRT W/NDLS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBI·March 12, 2020
REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 8
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 28, 2013
REALIZE ADJ GASTRIC BAND-C
FDA Adverse Event
Injury
·OBTECH MEDICAL SARL_·Product code LTI·December 17, 2010
ACCU-CHEK ® INFORM II TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 14, 2014
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·July 1, 2014