10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STERILE WATER FOR INHALATION FLEX BAG, USP
FDA 510(k)
FDA Class 2
·Anesthesiology
AMC
FDA UDI
Advantage Medical Electronics, LLC·00849593063395·NIBP Y Adapter, Female Threaded to Philips Female
INFINION CX
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 9, 2023
PASTEUR PIPET - STERILE 9, PASTEUR PIPET - STERILE 5 3/4, MODELS 16-PP-9, 16-PP-5.75
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CDMX
FDA 510(k)
FDA Class 2
·Dental
LUX 1440
FDA Adverse Event
Malfunction
·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 2, 2013
OT VERIO2 METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 16, 2014
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code FRN·May 2, 2011
Custom Kit, Sterile EO, Rx Only, Catalog No. K09-09815, Manufacturer: Merit Medical Systems, Inc. South Jordan, Utah 84095, USA,
FDA Recall
Terminated
·Merit Medical Systems, Inc.·Product code DQO·October 25, 2010