31 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814695·GENUMEDI SILVER SIZE VI
ELI 10 ELECTROCARDIOGRAPH MODEL ELI 10
FDA 510(k)
FDA Class 2
·Cardiovascular
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814640·GENUMEDI SILVER SIZE I
REPICCI II RESURFACING KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304447110·
DURAVENT
FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948005448·DURAVENT UNI 1 IC + 1 ICU, SIZE 6
Plateau Spacer System
FDA UDI
Life Spine, Inc.·00190837026035·PLATEAU Interbody, Straight, Bulleted, 10mm 22m...
ALTERNANAS PROCESSING SYSTEM, CH 2000 CARDIAC DIAGNOSTIC SYSTEM, HEARTWAVE ALTERNANS PROCESSING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
HI-TORQUE WHISPER LS GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, HI-TORQUE WHISPER MS GUIDE WIRE WITH HYDROCOAT HYDRO
FDA 510(k)
FDA Class 2
·Cardiovascular
TGS UKA SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC·Product code HSX·March 22, 2013
EPIPHANY
FDA UDI
PANTHEON SPINAL, LLC·B528100204041022060·#4 15 DEGREE CURVED DOWN CURETTE SHAFT
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·May 6, 2013
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL, INC·Product code HSX·February 12, 2014
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL, INC.·Product code HSX·September 25, 2014
INFUSE BONE GRAFT 12 MG
FDA Adverse Event
Injury
·MEDTRONIC·Product code NEK·May 1, 2014
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·September 10, 2013
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, LLC·Product code HSX·August 14, 2013
32MM I.D. 7MM OFFSET SIZE HH LINER USE WITH 50MM O.D. SIZE HH SHELL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·August 31, 2023
METRX
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code LXH·May 9, 2013
MELODY TRANSCATHER PULMONARY
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPV·September 19, 2014
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 19, 2011