BEUDAMED
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    Res-Q-Vac

    FDA UDI
    REPRO MED SYSTEMS, INC.·00659443001220·REPL NSC SOFT NS CC

    Res-Q-Vac

    FDA UDI
    REPRO MED SYSTEMS, INC.·00659443001824·PUMP FSP S0FT ALL CATH NS

    HIgH-Flo™ Needle Set

    FDA UDI
    REPRO MED SYSTEMS, INC.·00659443000421·26 Gauge Needle Sets - 4 needles - 14 mm

    BioCLIA Autoimmune Reagent Kit, AMA-M2

    Device
    EU IVDD · Eu Ivd General ·HOB Biotech Group Corp., Ltd.·On the market

    BioCLIA Autoimmune Control Set, AMA-M2

    Device
    EU IVDD · Eu Ivd General ·HOB Biotech Group Corp., Ltd.·On the market

    BioCLIA Autoimmune Calibrator Set, AMA-M2

    Device
    EU IVDD · Eu Ivd General ·HOB Biotech Group Corp., Ltd.·On the market

    BioCLIA Autoimmune Reagent Kit, AMA-M2

    Device
    EU IVDD · Eu Ivd General ·HOB Biotech Group Corp., Ltd.·On the market

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Percepta Bipolar CRT-P, Percepta Quadripolar CRT-P, Serena Bipolar CRT-P, Serena Quadripolar CRT-P, Solara Bipolar CRT-P

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC CARELINK MONITOR MODEL 2490C AND MODEL 2491 DDMA DEVICES

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·Astra S DR MRI IPG, Astra S SR MRI IPG, Astra XT DR MRI IPG, Astra XT SR MRI IPG, Azure S DR MRI IPG, Azure S SR MRI IPG

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC CARELINK MONITOR MODEL 2490C AND MODEL 2491 DMA SOFTWARE

    Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

    FDA Pre-Market Approval
    FDA Class 3 ·CONCERTO MODEL C154DWK

    X100 with Full Field Bone Marrow Aspirate (BMA) Application 2 X100HT with Full Field Bone Marrow Aspirate (BMA) Application

    FDA 510(k)
    FDA Class 2 ·Hematology

    D.I. WARE COMPANY

    FDA registration
    D.I. WARE COMPANY·1 product·🇭🇰 Hong Kong

    D.I. WARE COMPANY

    FDA registration
    D.I. WARE COMPANY·1 product·🇭🇰 Hong Kong

    D.I. WARE COMPANY

    FDA registration
    D.I. WARE COMPANY·1 product·🇭🇰 Hong Kong

    STAINLESS STEEL DEN. CROWN REMOVER & AMA./COMP.CAR

    FDA 510(k)
    FDA Class 1 ·Dental

    DISPOSABLE AMA STERILE DRAPE SHEET, CAT. NO. 5252

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

    LATEX EXAMINATION / TREATMENT GLOVES

    Device
    EU MDR · Eu Md Class 1 ·Guangzhou Jia Ming Rubber Products Co., LTD·On the market·32 countries

    AireMed

    FDA UDI
    Jiangmen Jia Mei Medical Products Co., Ltd.·06976323220064·