190 results · 23ms · Sources: EU EUDAMED, US FDA

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UNIDRIVE II PLUS DISPOSABLE TUBING SET

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526743700·ACHIMED ACHILLES SUPP SAND I

NEU-ION HEMODIALYIS WATER TREATMENT SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

MONARCH INFLATION SYRINGE; UNIVERSAL FLUID DISPENSING SYRINGE

FDA 510(k)
FDA Class 2 ·Cardiovascular

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCABOROUGH, INC.·Product code QJR·April 21, 2021

DEXTRUS 4136

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code NVN·March 26, 2013

UNIFY QUADRA CRT-D

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·August 19, 2014

SPEEDBAND SUPERVIEW SUPER 7, MODELS 4205

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code MND·March 17, 2011

35MM TAP

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·November 8, 2024

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 16, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·November 11, 2010

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 23, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·May 9, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 18, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 16, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 2, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·October 5, 2010

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 10, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 17, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 2, 2011