9 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EQUIPMENT SNAP KOVERS
FDA 510(k)
FDA Class 2
·Radiology
Hillrom™
FDA UDI
Baxter Medical Systems GmbH + Co. KG·00887761991378·Trumpf Medical/Medizin Leg section one part H V
Leg Sections
FDA UDI
Baxter Medical Systems GmbH + Co. KG·00887761970366·Leg section one part H V
DELTON ILLUMINATING PIT AND FISSURE SEALING
FDA 510(k)
FDA Class 2
·Dental
Sutter Bipolar Forceps-Calvian
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYNCARDIA COMPANION 2 DRIVER
FDA Adverse Event
Malfunction
·SYNCARDIA SYSTEMS, INC.·Product code LOZ·March 25, 2014
OMNIFIT PSL HA ACET SHELL
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·November 20, 2012
ASR TAP SLV ADAP 12/14 -1
FDA Adverse Event
Injury
·DEPUY INTL., LTD.·Product code KWA·September 29, 2010
Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.
FDA Enforcement
Class II
·Terminated·STERILMED, INC.·December 16, 2015