8 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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EMBRYOVIEWER SOFTWARE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
AF541
FDA UDI
Respironics, Inc.·00606959046634·AF541 Under the Nose Mask with Standard Elbow, ...
GRYPHON PEEK DS ANCHOR W/ ORTHOCORD, GRYPHON PEEK ANCHOR W/ ORTHOCORD
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFICATION TO SECTRA IDS5 RADIOLOGY WORKSTATION - VERSION 10.1
FDA 510(k)
FDA Class 2
·Radiology
ZELTIQ COOLCORE (6.3)
FDA Adverse Event
Injury
·ZELTIQ AESTHETICS INC.·Product code OOK·June 19, 2014
QUADRA ASSURA CRT-D, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·October 1, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·June 9, 2011