9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)
FDA 510(k)
FDA Class 2
·General Hospital
P.F.C. SIGMA
FDA UDI
DEPUY (IRELAND)·10603295233091·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING TC3 2....
RCT700
FDA 510(k)
FDA Class 2
·Radiology
VANGUARD REMOVABLE MOLDED POLY TIBIA
FDA 510(k)
FDA Class 2
·Orthopedic
PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·June 24, 2014
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)
FDA Adverse Event
Injury
·ALLERGAN·Product code LTI·February 12, 2013
SPRINT QUATTRO SECURE
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·January 13, 2011
Depuy P.F.C. E knee system, TC3 tibial insert; polyethylene tibial insert, Sz 2.5, 22.5 mm; Ref 96-0525.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005
UNKNOWN BEARING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·March 10, 2017