31 results · 21ms · Sources: EU EUDAMED, US FDA

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MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, WATCH BP OFFICE AFIB (TWIN200 AFS).

FDA 510(k)
FDA Class 2 ·Cardiovascular

ILIZAROV

FDA UDI
Smith & Nephew, Inc.·03596010030160·HALF RING - SMALL BONE FIXATOR 60MM

Clear Readers

FDA UDI
Diversified Products, Inc.·00842894121672·

SAV

FDA UDI
Diversified Products, Inc.·00037741210177·

Needle Guide

FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436102978·Sterile endocavity needle guide for use with Su...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450190012·

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780178866·Integra® Jarit® Metzenbaum-Nelson Scissors, 9-1...

Clear Readers

FDA UDI
Diversified Products, Inc.·00842894113523·

PSYCHEMEDICS RIA PHENCYCLIDINE ASSAY

FDA 510(k)
FDA Unclassified ·Unknown

RETCAM II

FDA 510(k)
FDA Class 2 ·Ophthalmic

VASO VIEW HEMOPRO

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 8, 2019

HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, MEDIUM, 12°

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 4, 2024

VASOVIEW HEMOPRO 2

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 13, 2019

ATLAS II PLUS DR

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 9, 2013

NATURALYTE

FDA Adverse Event
Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·May 24, 2011

HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, LARGE, 12°, STERILE, SINGLE USE

FDA Adverse Event
Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAS·May 24, 2023

HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, LARGE, 30°, STERILE, SINGLE USE

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·June 6, 2023

HF-RESECTION ELECTRODE, LOOP

FDA Adverse Event
Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAS·June 2, 2023

HEMOPRO 2 ADAPTOR

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·February 21, 2020