24 results · 30ms · Sources: EU EUDAMED, US FDA

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MICROMEDIC LH & FSH RIA KIT

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

NAR

FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209136575·

MASIMO ROOT MONITORING SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

INFINITY GAMMAXL AND SC 6802XL WITH THE SCIO GAS MODULE

FDA 510(k)
FDA Class 2 ·Anesthesiology

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

RADICAL-7

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·February 19, 2016

SEDLINE KIT

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code MWI·January 8, 2017

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·May 30, 2014

MYNX CADENCE VASCULAR CLOSURE DEVICE 5F

FDA Adverse Event
Malfunction ·ACCESSCLOSURE, INC.·Product code MGB·June 28, 2012

FULL RADIUS RESECTOR

FDA Adverse Event
Injury ·CONMED LINVATEC CORP.·Product code HRX·September 14, 2010

RADICAL-7

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·July 9, 2015

SEDLINE KIT

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code GWQ·July 21, 2017

ROOT

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code MWI·September 20, 2018

KIT, RADICAL-7 HANDHELD

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code DQA·May 10, 2019