MYSHELL LITE

FDA registration

IONISOS·1 product·🇫🇷 France

MyShell Lite

FDA registration

Perouse Medical·1 product·🇫🇷 France

MyShell Lite

FDA registration

LILMO Ltd·1 product·🇲🇺 Mauritius

SEDAT MYSHELL LITE

FDA 510(k)

FDA Class 2 ·Cardiovascular

k083472

FDA registration

BD SWITZERLAND SARL·1 product·🇨🇭 Switzerland

Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

FDA classification

FDA Class 2 ·Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

Hillrom™

FDA UDI

Baxter Medical Systems GmbH + Co. KG·00887761976108·Trumpf Medical/Medizin Pad upper back section G

Pads

FDA UDI

Baxter Medical Systems GmbH + Co. KG·00887761969056·Pad upper back section G

Regent

FDA UDI

SPINAL ELEMENTS·00840916115036·Regent ACP 4-Level, 72mm

Mammotome Biopsy System

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

MOSFET20

FDA registration

Best Theratronics Ltd.·1 product·🇨🇦 Canada

SchureMed

FDA UDI

SCHUERCH CORPORATION·00810014600116·30" SCHURE SPINE FRAME PAD

SchureMed

FDA UDI

SCHUERCH CORPORATION·00810014606194·Schure Spine Frame Pads

Synergy Health Sterilisation UK Ltd

FDA registration

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

PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50

FDA 510(k)

FDA Class 2 ·Radiology

POSI-LINK

FDA 510(k)

FDA Class 2 ·General Hospital

Accelerator, Linear, Medical

FDA classification

FDA Class 2 ·Accelerator, Linear, Medical

Set, Administration, Intravascular

FDA classification

FDA Class 2 ·Set, Administration, Intravascular