30 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Tempus Pro Patient Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
DJO SURGICAL
FDA UDI
Encore Medical, L.P.·00190446857716·SPECIAL, EXPRT REVISION HIP DISTAL STEM TRIAL, ...
MSI
FDA UDI
Modern Surgical Instruments LLC·B4192017460·
HHM
FDA UDI
Oticon A/S·05707131351487·G500 SC, BTE PP 13 2.4G 105 C090 TAR HHM
MSI
FDA UDI
Modern Surgical Instruments LLC·00810130202034·6" Vein Retractor, with Loop Handle
CODMAN
FDA UDI
Cerenovus, Inc.·10886704001980·CODMAN SLIM-LINE Aneurysm Clip Reinforcing Angl...
7450 RV2 MASK
FDA UDI
HANS RUDOLPH, INC.·00817136022505·7450S FACE MSK-HEADGEAR-CC1808
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776191863·VEIN RETRACTOR BLADE LENGTH WIDE
Symmetry Surgical
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482057704·Symmetry® Retractor, Custom Vein, 6 in
SQA V, SPERM QUALITY ANALYZER
FDA 510(k)
FDA Class 2
·Hematology
LIGHTSHEER PULSED DIODE ARRAY LASER SYSTEM (FAMILY OF PRODUCTS)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MERSILENE TAPE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code KDC·November 9, 2018
UNKNOWN COOL TIP ELECRTRODE
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·March 3, 2020
GE OEC 6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 21, 2008
HS III PROXIMAL SEAL SYSTEM 4.3MM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code DXC·August 4, 2011
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·June 28, 2013
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 20, 2012
SYNERGY
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 25, 2015
UNK - CONSTRUCTS: PHILOS PLATE/SCREWS
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HRS·June 10, 2021
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·April 9, 2019