16 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAP-ONE, MODEL TG-920P
FDA 510(k)
FDA Class 2
·Anesthesiology
Tiche PTA Balloon Dilatation Catheter
FDA UDI
BrosMed Medical Co.,Ltd.·06958481476156·
HYCARE LATEX EXAMINATION GLOVE, POWDERED
FDA 510(k)
FDA Class 1
·General Hospital
ASSAYED QCS 1,2, CAT. NOS. 970200, 970500
FDA 510(k)
FDA Class 1
·Clinical Chemistry
BD VACUTAINER BUFFERED SODIUM CITRATE (9NC) BLOOD COLLECTION TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·July 14, 2021
BD VACUTAINER BUFFERED SODIUM CITRATE BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·June 3, 2021
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·April 8, 2013
ENDEAVOR SPRINT RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·March 24, 2011
MESH - COMPOSIX KUGEL
FDA Adverse Event
Injury
·DAVOL ,INC., SUB C.R. BARD, INC.·Product code FTL·April 29, 2008
VITEK® 2 AST-N350
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·December 17, 2018
VITEK® 2 AST-N350
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·December 17, 2018
BD VACUTAINER BUFFERED SODIUM CITRATE (9NC) BLOOD COLLECTION TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·July 14, 2021
BD VACUTAINER BUFFERED SODIUM CITRATE (9NC) BLOOD COLLECTION TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·July 14, 2021
UNKNOWN KNEE TIBIAL TRAY
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·November 7, 2019
Thoratec HeartMate 3, LVAS Implant Kit, REF:106524INT, Sterile EO, RxOnly
FDA Enforcement
Class I
·Ongoing·Thoratec Corp.·May 8, 2024
Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly
FDA Enforcement
Class I
·Ongoing·Thoratec Corp.·May 8, 2024