GE Vivid I Ultrasound

FDA registration

BAY SHORE MEDICAL EQUIPMENT, LLC·3 products·🇺🇸 United States

GE Vivid I Portable

FDA registration

LBN MEDICAL A/S·3 products·🇩🇰 Denmark

GE VIVID I DIAGNOSTIC ULTRASOUND, GE VIVID Q DIAGNOSTIC ULTRASOUND

FDA 510(k)

FDA Class 2 ·Radiology

MAJ-1351

FDA registration

OLYMPUS MEDICAL SYSTEMS CORP.·4 products·🇯🇵 Japan

MAJ-1351

FDA registration

AOMORI OLYMPUS CO., LTD.·4 products·🇯🇵 Japan

XPERT MRSA Elution Reagent, Assay

FDA registration

VWR CHEMICALS, LLC·1 product·🇺🇸 United States

MAJ-1351

FDA registration

Aomori Olympus Co., Ltd. Distribution Center·4 products·🇯🇵 Japan

SANICURE BV

FDA registration

SANICURE BV·4 products·🇳🇱 Netherlands

MAJ-1351

FDA registration

SHIRAKAWA OLYMPUS CO., LTD.·4 products·🇯🇵 Japan

Bonastent Esophageal

FDA registration

THORACENT, INC.·1 product·🇺🇸 United States

COM-PATCH

FDA 510(k)

FDA Class 2 ·Neurology

MENICON PROGENT REMOVER

FDA 510(k)

FDA Class 2 ·Ophthalmic

System, Imaging, Pulsed Echo, Ultrasonic

FDA classification

FDA Class 2 ·System, Imaging, Pulsed Echo, Ultrasonic

Products, Contact Lens Care, Rigid Gas Permeable

FDA classification

FDA Class 2 ·Products, Contact Lens Care, Rigid Gas Permeable

Electrode, Cutaneous

FDA classification

FDA Class 2 ·Electrode, Cutaneous