Selectra slitter tool

FDA registration

BIOTRONIK SE & CO. KG·1 product·🇩🇪 Germany

SELECTRA SLITTER TOOL

FDA 510(k)

FDA Class 2 ·Cardiovascular

9300

FDA UDI

HANS RUDOLPH, INC.·00874750008896·9324 1410B W/9300 VLV & 9301

MODULITH SLK with MULTIVIEW option

FDA registration

STORZ MEDICAL AG·1 product·🇨🇭 Switzerland

SkinVibe 990

FDA registration

METTLER ELECTRONICS CORP.·4 products·🇺🇸 United States

MODULITH SLK with MULTIVIEW option

FDA registration

STORZ MEDICAL AMERICA, INC.·1 product·🇺🇸 United States

ANTISERA, LATEX AGGLUTINATION, CRYPTOCOCCUS NEOFORMANS

FDA registration

MONOCENT INC.·1 product·🇺🇸 United States

Kitazato OPU Needle with Connection Tube, model number Type 2

FDA registration

KITAZATO CORPORATION·1 product·🇯🇵 Japan

QUALITY TECH SERVICES, LLC

FDA registration

QUALITY TECH SERVICES, LLC·1 product·🇺🇸 United States

Kitazato OPU Needle with Connection Tube, model number Type 2

FDA registration

RADIA INDUSTRY CO., LTD.·1 product·🇯🇵 Japan

FLASH PTA BALLOON DILATATION CATHETER 5MM X 19MM X 135CM; FLASH PTA BALLOON DILATATION CATHETER 6MM X 19MM X 135CM

FDA 510(k)

FDA Class 2 ·Cardiovascular

STORZ MODULITH SLK LITHOTRIPTER WITH MULTIVIEW OPTION

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous

Lithotriptor, Extracorporeal Shock-Wave, Urological

FDA classification

FDA Class 2 ·Lithotriptor, Extracorporeal Shock-Wave, Urological

Catheter, Angioplasty, Peripheral, Transluminal

FDA classification

FDA Class 2 ·Catheter, Angioplasty, Peripheral, Transluminal