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

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SINGLE USE INSTRUMENT TRAY

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MEDITECH MODEL ABPM-04

FDA 510(k)
FDA Class 2 ·Cardiovascular

Ready-Fit

FDA 510(k)
FDA Unclassified ·Unknown

COULTER® ACT 5DIFF CAP PIERCE (CP)

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GKZ·February 8, 2013

PROMUS

FDA Adverse Event
Malfunction ·PROMUS·Product code NIQ·December 30, 2010

ENERGEN

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 22, 2014

PENTAX

FDA Adverse Event
Malfunction ·Product code CAL·July 21, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·February 16, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·October 22, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FGB·November 30, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 31, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·April 22, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 16, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·August 5, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 4, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·December 14, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·August 26, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·July 11, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·August 21, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·September 8, 2023