BEUDAMED
    313 results · 21ms · Sources: EU EUDAMED, US FDA

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    VANTAGE TITAN 3T

    FDA 510(k)
    FDA Class 2 ·Radiology

    RC Cem. Abutment

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600306214·

    NexxZr™ T / D-100-20-NT-D300-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271113702·

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981200954·Interbody, 11mm x 32mm x 16mm, 0 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981192969·Interbody, 11mm x 32mm x 16mm, 0 deg

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10885425321384·LACERATION SAFETY TRAY

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981208073·Trial, 11mm x 32mm x 16mm, 0 deg

    SONTEC BAYONET NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896021914·SONTEC BAYONET NEEDLE HOLDER TUNGSTEN CARBIDE S...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197303873·Wullstein Suction tube with luer Ø2,0mm...

    STRETCH VINYL EXAMINATION GLOVE POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ARTELON SURGICAL SUTURE

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

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·August 24, 2015

    IMP TM 4.7MM MTX FULL, 11.5MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·November 25, 2022

    IMP TM 4.7MM MTX FULL, 10

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026

    IMP TM 4.7MM MTX FULL, 10

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    UNKNOWN_KIE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·May 29, 2013

    IN TOUCH ZU

    FDA Adverse Event
    Injury ·STRYKER MEDICAL·Product code FNL·June 13, 2011

    Accell Evo3C Demineralized Bone Matrix, 5 cc, Model Number: 02-6000-050 , Lot Number: 132160. Product Usage: Accell Evo3c Demineralized Bone Matrix Putty is intended for filling voids and gaps in the skeletal system that are not intrinsic to the stability of the bony structure. Accell Evo3c is indicated for use as a bone graft extender in the spine, extremities and pelvis, or as a bone void filler in the extremities and pelvis. The voids or gaps may be surgically created defects or the result of traumatic injury to the bone.

    FDA Enforcement
    Class II ·Terminated·Integra LifeSciences Corp.·July 2, 2014

    IMP TM 4.1MM MTX FULL, 11.5MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·June 1, 2020