8 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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4F STERILE BALLOON-LESS, CATHETER 913-28
FDA 510(k)
FDA Class 2
·Cardiovascular
TDS ABUTMENT FOR NOBEL BIOCARE REPLACE
FDA 510(k)
FDA Class 2
·Dental
MEDIP PRO
FDA 510(k)
FDA Class 2
·Radiology
N/A
FDA UDI
Zimmer, Inc.·00889024192775·
ELLIPSE DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·May 5, 2014
EXTERNAL PULSE GENERATOR
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012
30327 12CC 100 UNIT HEP SYR {CAN} 2.5CC
FDA Adverse Event
Malfunction
·COVIDIEN·Product code NZW·July 20, 2010
MENTOR SILTEX ROUND MODERATE PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·March 21, 2018