11 results
·
25ms
·
Sources: EU EUDAMED, US FDA
PREPAX DILUKIT PLUS
FDA 510(k)
FDA Class 1
·Hematology
NA
FDA UDI
Zimmer, Inc.·00889024101999·
CONTOUR CURVED CUTTER STAPLER CS
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 13, 2006
DIGIMATCH ORTHODOC ROBODOC ENCORE SURGICAL SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
CURVED CUTTER STAPLER, MODELS CS40B, CS40G; RELOAD FOR CURVED STAPLER, MODELS CR40B, CR40G
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NA
FDA UDI
Zimmer, Inc.·00889024074033·
OT ULTRALINK METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 30, 2014
VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HAV IGM REAGENT
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code LOL·November 20, 2012
INTEGRATED APD SET W/CASSETTE3 PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 21, 2010
Colonoscope, Model Number PCF-H190DL.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·March 6, 2024
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