813 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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