BEUDAMED
    46 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    CLEARARCH

    FDA 510(k)
    FDA Class 2 ·Dental

    JOBST Bella Strong

    FDA UDI
    BSN MEDICAL, INC.·00035664012328·BSTRNG 20-30 GNT SZ 8 BL 1 EN FR ES

    OMNIPULSE HOLMIUM LASER SYSTEM, OMNIPULSE-MAX HOLMIUM LASER SYSTEM, MODEL 1210, 1210-VHP, 1500-A

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VIVAWAVE MICROWAVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 30, 2013

    Y-SHAPED BLOOD SET W/ PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·September 12, 2013

    SYNCHRON® ALT REAGENT, 2 X 200 TEST

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CKA·July 26, 2011

    Y-SHAPED BLOOD SET W/ PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code BRZ·September 13, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·August 6, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 17, 2013

    NDEHP Y-BLOOD SET W/FILTER PUMP 203CM

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·February 24, 2011

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·August 6, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 10, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 1, 2013

    SERI SURGICAL SCAFFOLD (US)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code OXF·August 28, 2014

    RESTORE RECHARGEABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·May 11, 2011

    SOLUSET 100X60

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 22, 2013

    SOLUSET 100X60

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 22, 2013

    KRD DEVICE, EMBOLIZATION, VASCULAR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·September 19, 2019

    SECONDARY SET CAIR CLAMP NON-DEHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·May 5, 2014