BEUDAMED
    29 results · 22ms · Sources: EU EUDAMED, US FDA

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    BLASTASSIST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Premier Crown Removers

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·00348783010152·CROWN REMOVER POINT 5

    SCANLAN® Titanium Forceps

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159018929·TITANIUM MICR SUTR TYING FCEPS RND HNDL CURV DI...

    SCANLAN® Titanium Forceps

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159011975·Micro Suture Tying Fcp, RH, Gerald type taper, ...

    SCANLAN® Titanium Forceps

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159036381·Micro Suture Tying Fcp, RH, Gerald type taper, ...

    SCANLAN® Titanium Forceps

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159033212·Micro Suture Tying Fcp, RH, 0.4mm curv DD platf...

    Vbeam 7MM Delivery System W/O DCD

    FDA UDI
    Candela Corporation·00817495022239·Delivery System Assembly

    SMART SHIELD NON-STERILE POWDER-FREE PEPPERMINT SCENTED GREEN LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PHOENIX HEMODIALYSIS DELIVERY SYSTEM, GAMBRO CARTRIDGE FOR HEMODIALYSIS BLOOD TUBING SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    9616240-2006-00341

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    9616240-2006-00332

    FDA Adverse Event
    Other ·Product code FII·June 1, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    9616240-2006-00339

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    9616240-2006-00340

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 2/14MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 16, 2021

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 2/14MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 26, 2023

    9616240-2006-00350

    FDA Adverse Event
    Malfunction ·Product code FII·June 23, 2006

    9616240-2006-00345

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    NA

    FDA UDI
    Zimmer, Inc.·00889024066069·

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 6, 2025