354 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ECT Cotton Bite Block- size Large, ECT Cotton Bite Block -size Medium
FDA 510(k)
FDA Class 2
·Neurology
AGXO
FDA UDI
Oticon A/S·05707131352255·G500 S, MINIRITE 312 2.4G C044 AGXO
OptoMonitor 3
FDA UDI
Opsens Inc·07540184013098·
24M - Tampa Electric Co.
FDA UDI
Certified Safety Manufacturing, Inc.·00766588013497·24M Tampa Electric Co.
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668113844·VISCO CANNULA 21GA ANGLE 8MM
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450156971·
EXELINT ALUMINUM HUB BLUNT NEEDLES
FDA 510(k)
FDA Class 2
·General Hospital
HYDRO-CAST BIS-ACRYL TEMPORARY CROWN AND BRIDGE MATERIAL, MODEL 98250
FDA 510(k)
FDA Class 2
·Dental
I-STAT PT/INRCARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code GJS·November 4, 2013
I-STAT PT/INRCARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code GJS·November 4, 2013
ATTAIN ABILITY PLUS
FDA Adverse Event
Malfunction
·MPRI·Product code OJX·February 9, 2017
ONE TOUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·October 10, 2002
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 3, 2011
SUREFLEX 200 LITHOTRIPSY FIBER
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·June 26, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014
MEDIUM SPECIMEN RETRIEVAL BAG, 100MMX150
FDA Adverse Event
Malfunction
·GENICON·Product code FMH·April 21, 2015
HMOD70000#QUADROX-ID
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 6, 2014
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 4, 2013
MYOCARDIAL LEAD
FDA Adverse Event
Injury
·MPRI·Product code DTB·April 10, 2014
MYOCARDIAL LEAD
FDA Adverse Event
Injury
·MPRI·Product code DTB·April 10, 2014