24 results
·
20ms
·
Sources: EU EUDAMED, US FDA
GREAT TOE IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496014164·MARILYN 70 SHEER, SIZE L, CAMEL, GRADUATED COMP...
Natus
FDA UDI
XLTEK·00382830016360·Natus Quantum Pin Box 129-192
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033567951·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033567944·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033567975·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033567937·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033567982·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033567968·
MODIFICATION TO THE EMIT II PLUS METHAQUALONE ASSAY, MODEL OSR9Q229
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ICG MODULE
FDA 510(k)
FDA Class 2
·Cardiovascular
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
OPTISENSE
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011
ICY HOT HEAT THERAPY PATCH
FDA Adverse Event
Other
·CHATTEM, INC.·Product code IMD·March 13, 2008
VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA
FDA Adverse Event
Malfunction
·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·August 14, 2018
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·February 4, 2021
L3O0200 - NATURA
FDA Adverse Event
Malfunction
·CONVATEC DOMINICAN REPUBLIC INC·Product code EXE·January 27, 2021
L3O0200 - NATURA
FDA Adverse Event
Malfunction
·CONVATEC DOMINICAN REPUBLIC INC·Product code EXE·January 27, 2021
L3O0200 - NATURA
FDA Adverse Event
Malfunction
·CONVATEC DOMINICAN REPUBLIC INC·Product code EXE·January 27, 2021