BEUDAMED
    95 results · 28ms · Sources: EU EUDAMED, US FDA

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    Bone Cement

    FDA Pre-Market Approval
    FDA Class 2 ·PALACOS R BONE CEMENT

    Bone Cement

    FDA Pre-Market Approval
    FDA Class 2 ·PALACOS R BONE CEMENT

    Bone Cement

    FDA Pre-Market Approval
    FDA Class 2 ·PALACOS R BONE CEMENT

    Bone Cement

    FDA Pre-Market Approval
    FDA Class 2 ·OSTEOPAL

    Bone Cement

    FDA Pre-Market Approval
    FDA Class 2 ·PALACOS R BONE CEMENT

    Bone Cement

    FDA Pre-Market Approval
    FDA Class 2 ·PALACOS E-FLOW (OSTEOPAL) BONE CEMENT

    SWANSON

    FDA UDI
    WRIGHT MEDICAL TECHNOLOGY, INC.·00840420190048·Finger Joint Sizer

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327004021·PEEK CUSTOMIZED CRANIAL IMPLANT KIT, M

    Greenwald Surgical Company, Inc.

    FDA UDI
    GRACE MANUFACTURING, INC.·10801334000400·McCrea Female Sound, Curved. 3/4-inch nominal b...

    D3

    FDA UDI
    DIAGNOSTIC HYBRIDS, INC.·30014613338598·HSV-1 Control Stock

    AVANOS MIC GASTROSTOMY FEEDING TUBE WITH ENFIT CONNECTORS

    FDA Adverse Event
    AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)·Product code KNT·January 26, 2023

    Burn-out Anti-rotation Cap

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118141433·Burn-out Anti-rotation Cap

    PANJE VOICE PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Implanted Fecal Incontinence Device

    FDA Pre-Market Approval
    FDA Class 3 ·AMS ACTICON NEOSPHINCTER

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·COBAS 4800 BRAF V600 MUTATION TEST

    LARIAT SUTURE DELIVERY DEVICE

    FDA Adverse Event
    Injury ·SENTREHEART INC.·Product code GAT·May 1, 2014

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (LARGE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·October 23, 2012

    SYSTEM 12 CROSSFIRE 10 28MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·August 16, 2010

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·cobas® BRAF V600 Mutation Test

    Implanted Fecal Incontinence Device

    FDA Pre-Market Approval
    FDA Class 3 ·ACTICON NEOSPHINCTER ARTIFICAL BOWEL SPHINCTER