41 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NATURELLE DAILY DISPOSABLE (HILAFILCON B) COSMETICALLY TINTED CONTACT LENS
FDA 510(k)
FDA Class 2
·Ophthalmic
Causse
FDA UDI
MEDTRONIC XOMED, INC.·00763000033361·PROSTHESIS 1112192 CAUSSE MUSHRM TOTAL
Causse
FDA UDI
MEDTRONIC XOMED, INC.·00681490033572·PROSTHESIS 1112192 CAUSSE MUSHRM TOTAL
n/a
FDA UDI
HANS RUDOLPH, INC.·00874750006175·4813 SERIES NON HTD PTM
INDISCAL DIGITAL MANOMETER
FDA 510(k)
FDA Class 2
·General Hospital
DEFIBRILLATOR ANALYZER - DA-2006P
FDA 510(k)
FDA Class 2
·Cardiovascular
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·April 1, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·April 1, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·July 2, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·PFIZER, INC.·Product code QJR·May 8, 2023
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·February 28, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·May 19, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·January 16, 2023
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 7, 2022
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·December 15, 2015
STENT CORONARY
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code MAF·May 14, 2013
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code LZG·September 23, 2014
OT ULTRALINK METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·June 3, 2011
INSPIRA TEXTURED SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·January 2, 2024
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·January 20, 2022