25 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DM SLEEVE
FDA 510(k)
FDA Class 2
·General Hospital
Infinity-Lock 7
FDA UDI
XIROS LTD·05060267132567·
10MM TAP Cann Hud-Mod
FDA UDI
Osteocentric Technologies, Inc.·00810097801226·10MM TAP Cann Hud-Mod
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515010437·Basket for Half Size Container 9.7 x 9.7 x 2.1"
Reicodent
FDA UDI
devemed GmbH·04061644045990·EXTRACT 1100 - Extracting forceps # 2
Incisors ...
VERIDIAN
FDA UDI
VERIDIAN HEALTHCARE LLC·00845717000277·Provident Aneroid Sphygmomanometer, Large Adult
Reicodent
FDA UDI
devemed GmbH·04061644046010·EXTRACT 1100 - Extracting forceps # 2
Incisors ...
Reicodent
FDA UDI
devemed GmbH·04061644046003·EXTRACT 1100 - Extracting forceps # 2
Incisors ...
PARSET PRIMARY SET WITH CHECK VALVE, MODEL A10002E
FDA 510(k)
FDA Class 2
·General Hospital
ANTERIOR CRUCIATE LIGAMENT (ACL) INSTRUMENT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Eclipse Mini
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522130328·ECLIPSE MINI ECG SENSOR
KENEX
FDA UDI
KENEX (ELECTRO-MEDICAL) LIMITED·05055449403085·312/E-021/102 Table Shield 114cm with Rail 10mm...
Optimotion Blue CR HCCR Total Knee System
FDA UDI
OPTIMOTION IMPLANTS LLC·B6961014P0211020·CR Tibial Insert, UHMWPE + Vitamin E, Size 2, ...
PORTEX SPINAL ANESTHESIA TRAYS
FDA Adverse Event
Injury
·SMITHS MEDICAL ASD, INC.·Product code CAZ·March 15, 2013
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 16, 2011
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·March 27, 2008
SPECIFY
FDA Adverse Event
Injury
·NEURO - VILLALBA·Product code LGW·November 26, 2015
GLUCOSE SENSOR FREESTYLE LIBRE 2
FDA Adverse Event
Injury
·ABBOTT DIABETES CARE INC.·Product code MDS·January 19, 2022
ARCTIC FRONT ADVANCE® CARDIAC CRYOABLATION CATHETER
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code OAE·March 14, 2022
HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP
FDA Adverse Event
Injury
·HEARTWARE, INC.·Product code DSQ·September 13, 2021