BEUDAMED
    117 results · 20ms · 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.

    Chromogenic In Situ Hybridization, Nucleic Acid Amplification, Her2/Neu Gene, Breast Cancer

    FDA Pre-Market Approval
    FDA Class 3 ·SPOT-LIGHT HER2 CISH KIT

    Chromogenic In Situ Hybridization, Nucleic Acid Amplification, Her2/Neu Gene, Breast Cancer

    FDA Pre-Market Approval
    FDA Class 3 ·SPOT-LIGHT HER2 CISH KIT

    Chromogenic In Situ Hybridization, Nucleic Acid Amplification, Her2/Neu Gene, Breast Cancer

    FDA Pre-Market Approval
    FDA Class 3 ·SPOT-LIGHT HER2 CISH KIT

    Chromogenic In Situ Hybridization, Nucleic Acid Amplification, Her2/Neu Gene, Breast Cancer

    FDA Pre-Market Approval
    FDA Class 3 ·SPOT-LIGHT HER2 CISH KIT

    Avitene

    FDA UDI
    Davol Inc.·00801741010545·Avitene Ultrafoam, 8 cm x 12.5 cm (3-1/8" x 5")...

    EASYLIFE

    FDA UDI
    Respironics, Inc.·00606959027831·EasyLife Mask w/Headgear, Petite, Japan

    Copper Ni-Ti - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989025446·COPPER NITI 27 BAF 14 DIA U/S PK10

    OptiLIF Endo, Direct Visualization System

    FDA UDI
    SPINEOLOGY INC.·M7401050040·TF Endo Tubular Retractor, 6.6mm x 163mm x 40° ...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955933530·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955934148·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955932922·Percutaneous Transluminal Angioplasty Balloon C...

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981172916·L Con, Side-Loading, R, 8mm, 40mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410500400·Anterior Closing Wedge Osteotomy Guide, 50mm x ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420500400·Anterior Lateral Wedge Osteotomy Guide, 50mm x ...

    Sensica UO

    FDA UDI
    ADAPTEC MEDICAL DEVICES LLC·00854003008002·Automated urine meter system for continuous mon...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710400500400·Anterior Dome Osteotomy Guide, 50mm x 40mm

    MS-753 MARS INFLATE-READ BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HAND PK, MID 050040, GAUZE 4X4 XRAY RFD

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, INC.·Product code OJH·December 22, 2022

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·HYDRO THERMABLATOR ENDOMETRIAL ABLATION SYSTEM

    Sharps Needle Destruction Device

    FDA Pre-Market Approval
    FDA Class 2 ·THE DISINTEGRATOR INSULIN NEEDLE DESTRUCTION DEVICE