7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EMPTY I.V. CONTAINER
FDA 510(k)
FDA Class 2
·General Hospital
PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ASR TAP SLV ADAP 12/14 -1
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 15, 2013
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·December 6, 2010
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 5, 2014
Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.
FDA Enforcement
Class I
·Terminated·CareFusion 303, Inc.·August 26, 2015