29 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RANDOX THEOPHYLLINE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040012024·Zirlux 16+ A4 95X18
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033327777·
Ambu
FDA UDI
Bosma Enterprises·10818634025149·Ambu aScope 4 Cysto 5/Box
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033327746·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033327753·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033327760·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033327739·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033327722·
PARADIGM QUICK-SET INFUSION SET
FDA 510(k)
FDA Class 2
·General Hospital
PERIOLASE ND:YAG DENTAL LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BILATERAL DOUBLE BALLOON SET
FDA Adverse Event
Malfunction
·PAJUNK GMBH MEDIZINTECHNOLOGIE·Product code KOG·December 7, 2006
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code OUT·March 28, 2017
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA·Product code OUT·March 28, 2017
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 19, 2013
3 MOTOR ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 9, 2011
GE OEC 2800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC·Product code JAA·March 11, 2008
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code OUT·March 28, 2017
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code OUT·March 28, 2017
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code OUT·March 28, 2017