POWERFLEX PRO Percutaneous Transluminal Angioplasty Catheter

FDA registration

Nitinol Devices & Components Costa Rica, S. R. L.·1 product·🇨🇷 Costa Rica

Synergy Health AST, SRL

FDA registration

Synergy Health AST, SRL·1 product·🇨🇷 Costa Rica

ISOMEDIX OPERATIONS INC

FDA registration

ISOMEDIX OPERATIONS INC·1 product·🇺🇸 United States

Powerflex Pro Percutaneous Transluminal Angioplasty Catheter

FDA registration

Cordis US Corp.·1 product·🇺🇸 United States

POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

9300

FDA UDI

HANS RUDOLPH, INC.·00817136020174·9342 9324 LESS 9301 HD CNTRL

Hypodermic Needle-Single Lumen K-Pack Surshield Needle 27G x 1/2

FDA registration

Sterigenics Belgium Petit Rechain S.A.·1 product·🇧🇪 Belgium

27G X 1/2

FDA registration

TERUMO EUROPE N.V.·1 product·🇧🇪 Belgium

Gilbralt Cannulated Facet Screw

FDA registration

Choice Spine·1 product·🇺🇸 United States

27G X 1/2

FDA registration

Terumo Medical Canada, Inc.·1 product·🇨🇦 Canada

MEXPO INTERNATIONAL, INC.

FDA registration

MEXPO INTERNATIONAL, INC.·1 product·🇺🇸 United States

Alcon Research, LLC

FDA registration

Alcon Research, LLC·1 product·🇺🇸 United States

RMS CO.

FDA registration

RMS CO.·3 products·🇺🇸 United States

COMMUNIFY PACS VIEWER

FDA 510(k)

FDA Class 2 ·Radiology

DIAMEDIX IS-ANTI-GLIADIN IGA TEST SYSTEM

FDA 510(k)

FDA Class 2 ·Immunology

Catheter, Angioplasty, Peripheral, Transluminal

FDA classification

FDA Class 2 ·Catheter, Angioplasty, Peripheral, Transluminal

Antibodies, Gliadin

FDA classification

FDA Class 2 ·Antibodies, Gliadin

System, Image Processing, Radiological

FDA classification

FDA Class 2 ·System, Image Processing, Radiological