28 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Scanostics UTI Check Application Test System
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780130499·Integra® Jarit® Yankauer Suction Tube, 8-1/4", ...
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776379384·Guilford-Wright Double-Edged Sickle Knife, 7mm,...
Ni-Ti - Archwire
FDA UDI
ORMCO CORPORATION·00889989029802·ARCH REV.CURVE NITI LO18 DIA. PK10
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776079413·Yankauer Suction Tube, Small
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776163792·VAN BUREN URETH SNDS FR
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197066600·Desmarres Hand Held Retraktor
18mm, ...
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973107231·TRIAL 90-SRK-170118 POLY UCCS 1X18MM
OTOGRAM, CA3350
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
STIMTRODE SINGLE USE NERVE STIMULATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
ONE TOUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·March 12, 2002
U BY KOTEX UNKNOWN : TAMPON, MENSTRUAL, UNSCENTED : HEB
FDA Adverse Event
Malfunction
·BERRY PLASTICS QINGDAO LTD.·Product code HEB·October 31, 2022
U BY KOTEX : TAMPON, MENSTRUAL, UNSCENTED : HEB
FDA Adverse Event
Malfunction
·BERRY PLASTICS QINGDAO LTD.·Product code HEB·January 5, 2022
U BY KOTEX UNKNOWN : TAMPON, MENSTRUAL, UNSCENTED : HEB
FDA Adverse Event
Malfunction
·BERRY PLASTICS QINGDAO LTD.·Product code HEB·June 28, 2023
Widex
FDA UDI
Widex A/S·05706069923896·WIDEX MOMENT MBB3D 30 (Tech black)
Widex
FDA UDI
Widex A/S·05706069897715·WIDEX EVOKE E-FP (Tech Black ) 30, Telecoil, Vo...
Widex
FDA UDI
Widex A/S·05706069896084·WIDEX EVOKE E-FA (Tech Black ) 30, Telecoil, Vo...
Widex
FDA UDI
Widex A/S·05706069787740·WIDEX EVOKE E-FM (Tech Black ) 30, RC coil
RAD-57 CONFIGURABLE PULSE CO-OXIMETER
FDA Adverse Event
Malfunction
·MASIMO - 40 PARKER·Product code DQA·June 24, 2019
PRESSURE WIRE AERIS G8
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, COSTA RICA LTDA·Product code DXO·March 28, 2018