BEUDAMED
    21 results · 49ms · Sources: EU EUDAMED, US FDA

    Sol-M Luer Lock Syringe without Needle

    FDA registration
    Sol-Millennium Medical, Inc.·1 product·🇺🇸 United States

    Sol-M Luer Lock Syringe without Needle

    FDA registration
    Sol-Millennium Swiss R&D Center SA·1 product·🇨🇭 Switzerland

    Sol-M Luer Lock Syringe without Needle

    FDA registration
    Sol-Millennium Canada, INC.·1 product·🇨🇦 Canada

    Sol-M Luer Lock Syringe without Needle

    FDA registration
    SHANGHAI SOL-MILLENNIUM MEDICAL PRODUCTS CO, LTD·1 product·🇨🇳 China

    Sol-M Luer Lock Syringe without Needle

    FDA registration
    Sol-Millennium Europe Sp. z o. o.·1 product·🇵🇱 Poland

    SOL-KL (SHANGHAI) MEDICAL PRODUCTS COMPANY LIMITED

    FDA registration
    SOL-KL (SHANGHAI) MEDICAL PRODUCTS COMPANY LIMITED·1 product·🇨🇳 China

    Sol-M Luer Lock Syringe without Needle

    FDA registration
    ZHEJIANG LONGDE PHARMACEUTICAL Co., Ltd·1 product·🇨🇳 China

    Sol-M Luer Lock Syringe without Needle

    FDA registration
    SOL-MILLENNIUM MEDICAL HK LIMITED·1 product·🇭🇰 Hong Kong

    CYDONIA PHARMA SL

    FDA registration
    CYDONIA PHARMA SL·1 product·🇪🇸 Spain

    Sol-M Luer Lock Syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STRATAFIX™ Spiral MONOCRYL™ Plus Unidirectional Knotless Tissue Control Device

    FDA registration
    ETHICON, LLC·1 product·🇺🇸 United States

    STRATAFIX™ Spiral MONOCRYL™ Plus Unidirectional Knotless Tissue Control Device

    FDA registration
    ETHICON, LLC.·1 product·🇺🇸 United States

    STRATAFIX™ Spiral MONOCRYL™ Plus Unidirectional Knotless Tissue Control Device

    FDA registration
    ETHICON, INC.·1 product·🇺🇸 United States

    Elos Accurate Pre-milled Blank

    FDA registration
    ELOS MEDTECH PINOL A/S·2 products·🇩🇰 Denmark

    STRATAFIX™ Spiral MONOCRYL™ Plus Unidirectional Knotless Tissue Control Device

    FDA registration
    ETHICON, INC.·1 product·🇺🇸 United States

    STRATAFIX™ Spiral MONOCRYL™ Plus Unidirectional Knotless Tissue Control Device

    FDA registration
    ETHICON, INC.·1 product·🇺🇸 United States

    REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PROSPERA OTC TENS ELECTRONIC PULSE MASSAGER

    FDA 510(k)
    FDA Class 2 ·Neurology

    Syringe, Piston

    FDA classification
    FDA Class 2 ·Syringe, Piston

    Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

    FDA classification
    FDA Class 1 ·Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment