28 results · 26ms · Sources: EU EUDAMED, 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