30 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TANDEMHEART PUMP
FDA 510(k)
FDA Class 2
·Cardiovascular
Nogama
FDA UDI
SILMET LTD·07290012207082·Dental Amalgam Capsules
JOBST ActiveWear
FDA UDI
BSN MEDICAL, INC.·00035664104931·ACTIVE WEAR 20-30 MM HG KNEE HIGH CLOSED TOE SM...
DONJOY
FDA UDI
DJO, LLC·00190446257189·DONJOY ICEMAN CLEARCUBE
DONJOY
FDA UDI
DJO, LLC·00190446280606·DONJOY ICEMAN CLEARCUBE, EASTERN MAINE MEDICAL
DONJOY
FDA UDI
DJO, LLC·00190446738329·ICEMAN CLEAR3 COLD THERAPY UNIT, ORTHO RHODE IS...
AIRCAST
FDA UDI
DJO, LLC·00190446298243·DONJOY ICEMAN CLEARCUBE, ORTHO NY
DONJOY
FDA UDI
DJO, LLC·00190446220312·DONJOY ICEMAN CLEARCUBE, K. PERMANENTE
SUPERDIMENSION MARKER DELIVERY KIT
FDA 510(k)
FDA Class 2
·Radiology
ADVANCED GLASS IONOMER (K-130) RESTORATIVE
FDA 510(k)
FDA Class 2
·Dental
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·May 14, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·September 23, 2014
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·April 25, 2011
CAPIOX RX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DTZ·May 26, 2023
CAPIOX RX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 20, 2018
CAPIOX RX OXYGENATOR
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 31, 2024
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DTZ·January 31, 2024
CAPIOX®RX
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 9, 2024
CAPIOX RX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 5, 2018
BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 29, 2019