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

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SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000

FDA 510(k)
FDA Class 2 ·Cardiovascular

BUTTERFLY PLATE FUNCTION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE

FDA 510(k)
FDA Class 2 ·General Hospital

CADD

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·March 23, 2022

CADD MEDICATION CASSETTE

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·July 14, 2022

CADD

FDA Adverse Event
Malfunction ·NULL·Product code FPA·August 17, 2021

CADD MEDICATION CASSETTES

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·June 6, 2022

ENDOTAK RELIANCE

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVY·April 8, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 22, 2011

GENICON SUCTION IRRIGATION SYSTEM

FDA Adverse Event
Malfunction ·GENICON·Product code GCX·May 7, 2008

BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

FDA Adverse Event
Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·July 31, 2019

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·September 17, 2012

Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

FDA Enforcement
Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012

The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018