13 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MRIdian Linac System
FDA 510(k)
FDA Class 2
·Radiology
BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·August 9, 2021
CLAVICLE PIN TAP
FDA UDI
Biomet Orthopedics, LLC·00887868023804·
CLAVICLE PIN TAP
FDA UDI
Biomet Orthopedics, LLC·00887868078491·
CLAVICLE PIN TAP
FDA UDI
Biomet Orthopedics, LLC·00887868078507·
CLAVICLE PIN TAP
FDA UDI
Biomet Orthopedics, LLC·00887868078484·
BREATHING CIRCUIT FILTER
FDA 510(k)
FDA Class 2
·Anesthesiology
HUMID-VENT HEPA
FDA 510(k)
FDA Class 2
·Anesthesiology
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·August 8, 2011
JUVEDERM ULTRA PLUS XC TSK US
FDA Adverse Event
Injury
·ALLERGAN·Product code LMH·October 24, 2014
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 9, 2013
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·August 15, 2017
BV Pulsera with Software Release 2.3-A mobile, diagnostic X-ray image acquisition and viewing system. Model Number: 718095
FDA Enforcement
Class II
·Ongoing·Philips North America Llc·December 15, 2021