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