BEUDAMED
    20 results · 50ms · Sources: EU EUDAMED, US FDA

    Perfix Spinal System

    FDA registration
    CG MedTech USA, Inc.·2 products·🇺🇸 United States

    LDR MEDICAL

    FDA registration
    LDR MEDICAL·2 products·🇫🇷 France

    Perfix Spinal System

    FDA registration
    CG MedTech Co., Ltd.·2 products·🇰🇷 South Korea

    PERFIX SPINAL SYSTEM, MODEL SNA4530-9610, SNM4530-9610, SN3020 (TOTAL: 549)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989026863·ARCH P/F EDG.RECT.LO170 X250 PK10

    SYNTHES TI-15 MO LOCKING DISTAL RAD

    FDA registration
    Synthes (USA) Products LLC·1 product·🇺🇸 United States

    SYNTHES TI-15 MO LOCKING DISTAL RADIUS PLATING SYSTEM

    FDA registration
    EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

    Amphenol Cable and Interconnect Technologies Asia Pacific Ltd.

    FDA registration
    Amphenol Cable and Interconnect Technologies Asia Pacific Ltd.·1 product·🇭🇰 Hong Kong

    APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

    FDA registration
    SYNTHES GMBH·1 product·🇨🇭 Switzerland

    Amphenol Medical Technologies (Dongguan) Co., Ltd.

    FDA registration
    Amphenol Medical Technologies (Dongguan) Co., Ltd.·1 product·🇨🇳 China

    Jabil Inc. (Elmira)

    FDA registration
    Jabil Inc. (Elmira)·1 product·🇺🇸 United States

    Orthosis, Spondylolisthesis Spinal Fixation

    FDA classification
    FDA Class 2 ·Orthosis, Spondylolisthesis Spinal Fixation

    Stryker Aria Pneumatic System

    FDA registration
    STRYKER IRELAND LTD., INSTRUMENTS DIVISION·1 product·🇮🇪 Ireland

    Synergy Health Sterilisation UK Ltd

    FDA registration
    Synergy Health Sterilisation UK Ltd·1 product·🇬🇧 United Kingdom

    Cryosolutions

    FDA registration
    NEW MEDICAL TECHNOLOGIES GMBH·1 product·🇨🇭 Switzerland

    2.1mm Tapered Titanium Router (M-IF-220)

    FDA registration
    ORCHID UNIQUE·1 product·🇺🇸 United States

    OLYMPUS SUCTION PUMP, MODEL KV-5

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

    HEARTSTREAM XL DEFIBRILLATOR/MONITOR, MODEL M4735A

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Apparatus, Suction, Ward Use, Portable, Ac-Powered

    FDA classification
    FDA Class 2 ·Apparatus, Suction, Ward Use, Portable, Ac-Powered

    Automated External Defibrillators (Non-Wearable)

    FDA classification
    FDA Class 3 ·Automated External Defibrillators (Non-Wearable)