25 results · 21ms · Sources: EU EUDAMED, 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