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