BEUDAMED
    27 results · 22ms · 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.
    Filters Regulation: Us FDA ×

    ITOTAL CRUCIATE RETAINING (CR) KNEE REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Gyrus ACMI

    FDA UDI
    Gyrus ACMI, LLC·00821925014237·SHEA CUP PISTON SMALL, RIGHT 6.0 MM LENGTH FLUO...

    AGXO

    FDA UDI
    Oticon A/S·05707131270047·H160, DESIGNRITE 10 WL SIL AGXO

    ENTOPIC CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896023895·ENTOPIC CLAMP SERRATED TIP DOUBLE ARTICULATING ...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776170516·Clamp Wilson Entoptic Double Articulating Class...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197054720·Mixter Gall Duct Clamp Forceps 190mm,...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197054690·MIXTER Dissecting Forceps 155mm,...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197382922·Mixter Dissecting Forceps 41.0cm...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197382915·Mixter Dissecting Forceps 35.5cm...

    BIONIME RIGHTEST BLOOD GLUCOSE MONITORING SYSTEM, MODEL GM650

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DERMABOND NX ADHESIVE MODEL: DNX6, DNX12

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

    OLYMPUS EMPOWER H65

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM S.P.A.·Product code GEX·May 19, 2022

    HISTOACRYL FLEXIBLE PACK 5

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code MPN·December 3, 2019

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 31, 2013

    VOLUSON E8

    FDA Adverse Event
    Death ·GE HEALTHCARE·Product code IYO·June 21, 2011

    *

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·June 12, 2008

    POLARIS SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020

    PEDICLE SCREW UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021