QUESTUS

FDA registration

WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

QUESTUS POLYESTER SUTURE SOFT TISSUE ANCHOR SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

YS, YES STUDIO, DonnaMax, Bioswiss. Model: K1, K2, K3, K4, K5, K6, K7, K8, K9, 6200, 6201, 6202, 6203, 6204, 6205, 6206, 6207

FDA registration

CORAL HEALTHCARE PRODUCTS MANUFACTURER CO., LTD.·1 product·🇨🇳 China

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·1 product·🇺🇸 United States

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·1 product·🇺🇸 United States

BOSTON SCIENTIFIC CORPORATION

FDA registration

BOSTON SCIENTIFIC CORPORATION·1 product·🇺🇸 United States

Boston Scientific Limited

FDA registration

Boston Scientific Limited·1 product·🇮🇪 Ireland

PBD-421-1009

FDA registration

Aomori Olympus Co., Ltd. Distribution Center·1 product·🇯🇵 Japan

PBD-421-1009

FDA registration

OLYMPUS MEDICAL SYSTEMS CORP.·1 product·🇯🇵 Japan

PBD-421-1009

FDA registration

AOMORI OLYMPUS CO., LTD.·1 product·🇯🇵 Japan

Maverick XL Percutaneous Transluminal Coronary Angioplasty Monorail Dilatation Cathete

FDA 510(k)

FDA Class 2 ·Cardiovascular

20.1-INCH (51CM) COLOR LCD MONITOR CDL2010A (CCL204)

FDA 510(k)

FDA Class 2 ·Radiology

Fastener, Fixation, Nondegradable, Soft Tissue

FDA classification

FDA Class 2 ·Fastener, Fixation, Nondegradable, Soft Tissue

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA classification

FDA Class 2 ·Catheters, Transluminal Coronary Angioplasty, Percutaneous

System, Image Processing, Radiological

FDA classification

FDA Class 2 ·System, Image Processing, Radiological