24 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LIFEPAK 1000 DEFIBRILLATOR
FDA 510(k)
FDA Class 3
·Cardiovascular
LIFEPAK(R) 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015
LIFEPAK® 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019
K-Systems
FDA UDI
RESEARCH INSTRUMENTS LIMITED·05060554120017·Assisted Reproduction Accessories
BARRAQUER IRIS SPATULA
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896072688·BARRAQUER IRIS SPATULA ROUND CURVED SMOOTH BLAD...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702256604·ELVAREX 2/THIGH HIGH/SLANT, CLOSED TOE, E-VERSI...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702557206·ELVAREX 3/KNEE HIGH/OPEN TOE-ELEPHANTIASIS-VERS...
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780165125·Integra® Jarit® Skinner Needle and Tissue Force...
BARRAQUER IRIS SPATULA
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896013292·BARRAQUER IRIS SPATULA ROUND SMOOTH CURVED BLAD...
UniTip Catheter
FDA UDI
Unisensor AG·07640172971369·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973233·
POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
SIMPLYGO BREAST PUMP
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100910·L Tibial Baseplate Cemented Stemmed Sz 6
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101771·L Tibial Baseplate Cemented Keeled Sz 6
THOMAS TREVISANI
FDA UDI
The Wells Johnson Company·B458201226000·Cannula, Trevisani, specify length, diameter an...
3I T3® TAPERED IMPLANT 4/3 X 11.5MM
FDA Adverse Event
Injury
·BIOMET 3I·Product code DZE·May 20, 2025
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 9, 2021
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·May 21, 2013
RESTORE ADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 26, 2014