813 results · 33ms · Sources: EU EUDAMED, US FDA

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PMD-200 Finger Probe

FDA UDI
MEDASENSE BIOMETRICS LTD·07290017287294·

MEDLINE NEEDLE,30GX0.5"REG,BEVEL

FDA Adverse Event
Malfunction ·MEDLINE INDUSTRIES, INC.·Product code FMF·August 31, 2023

ZYNO PUMPS

FDA Adverse Event
Injury ·ZYNO MEDICAL, LLC·Product code FRN·May 21, 2024

RADIESSE (+)

FDA Adverse Event
Injury ·MERZ N AMERICA·Product code LMH·May 20, 2015

PREGNANCY TEST

FDA Adverse Event
UNK·Product code LCX·February 14, 2018

TRUERESULT METER

FDA Adverse Event
Other ·TRIVIDIA·Product code NBW·June 21, 2016

ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

FDA Adverse Event
Injury ·ZYNO MEDICAL, LLC·Product code FRN·July 9, 2024

NANOKNIFE SYSTEM

FDA Adverse Event
Injury ·ANGIODYNAMICS·Product code OAB·March 15, 2013

APPOSE ULC

FDA Adverse Event
Malfunction ·COVIDIEN·Product code GDT·July 25, 2023

STANDARD INSERTION HANDLE

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code LXH·November 9, 2022

ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

FDA Adverse Event
Injury ·ZYNO MEDICAL, LLC·Product code FRN·January 21, 2025

MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAN·June 5, 2025

TELEFLEX MEDICAL AC3 OPTIMUS INTRA AORTIC BALLOON PUMP

FDA Adverse Event
Injury ·TELEFLEX INCORPORATED·Product code DSP·March 26, 2026

EVERFLO OXYGEN CONCENTRATOR

FDA Adverse Event
Death ·PHILIPS HEALTHCARE·Product code CAW·March 13, 2014

REMEDE SYSTEM

FDA Adverse Event
Injury ·REMEDE SYSTEM·Product code PSR·January 15, 2026

TRUERESULT

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·July 31, 2018

IMPLANTED PERCUTANEOUS CATHETER

FDA Adverse Event
Malfunction ·BARD ACCESS SYSTEMS·Product code LJS·August 23, 2019

DOCTOR'S DATA URINE TOXIC & ESSENTIAL ELEMENTS (PROVOKED / POST-PROVOCATION)

FDA Adverse Event
Malfunction ·DOCTOR'S DATA INC.·Product code OIE·November 24, 2025

SENSATION PLUS 7.5FR. 40CC IAB & ACCESSORIES

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·April 30, 2024

HF SENSOR DELIVERY SYSTEM

FDA Adverse Event
Injury ·Product code MOM·January 25, 2024