Endophys Blood Pressure Monitor

FDA registration

RJC ENTERPRISES, LLC.·1 product·🇺🇸 United States

Endophys Blood Pressure Monitor

FDA 510(k)

FDA Class 2 ·Cardiovascular

Computer, Blood-Pressure

FDA classification

FDA Class 2 ·Computer, Blood-Pressure

CoRoent

FDA UDI

Nuvasive, Inc.·00887517730886·CoRoent XL+, 9x18x45mm 15°

PORTEX GRIGGS PERCUTANEOUS DILATION BLUS TRACHY KIT WITH DRUGS SIZE 9MM 2/CA Portex Griggs Percutaneous Blu Line Tra

FDA registration

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

PORTEX GRIGGS PERCUTANEOUS DILATION BLUS TRACHY KIT WITH DRUGS SIZE 9MM 2/CA Portex Griggs Percutaneous Blu Line Tra

FDA registration

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

PORTEX GRIGGS PERCUTANEOUS DILATION BLUS TRACHY KIT WITH DRUGS SIZE 9MM 2/CA Portex Griggs Percutaneous Blu Line Tra

FDA registration

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

PORTEX GRIGGS PERC TRACH KITS

FDA registration

ICU Medical, Inc.·1 product·🇺🇸 United States

PORTEX GRIGGS PERC TRACH KITS

FDA registration

ICU Medical Healthcare Manufacturing S.A. de C.V.·1 product·🇲🇽 Mexico

Calprest

FDA registration

EUROSPITAL S.P.A.·1 product·🇮🇹 Italy

Isomedix Operations Inc.

FDA registration

Isomedix Operations Inc.·1 product·🇺🇸 United States

PORTEX GRIGGS PERC TRACH KITS

FDA registration

ICU Medical Czech Republic a. s.·1 product·🇨🇿 Czechia

PORTEX GRIGGS PERC TRACH KITS

FDA registration

ICU Medical, Inc.·1 product·🇺🇸 United States

OsteoMed

FDA UDI

OSTEOMED LLC·00845694045100·PrimaLIF LLIF PEEK Implant, 9mm X 22mm X 45mm, ...

Elecsys CYFRA 21-1 CalSet

FDA registration

ROCHE DIAGNOSTICS GMBH·3 products·🇩🇪 Germany

Sonablate

FDA registration

Focus Surgery, Inc.·1 product·🇺🇸 United States

PORTEX PERCUTANEOUS TRACHEOSTOMY KIT

FDA 510(k)

FDA Class 2 ·Anesthesiology

FUSE PLIF CAFE

FDA 510(k)

FDA Class 2 ·Orthopedic

Tube, Tracheostomy (W/Wo Connector)

FDA classification

FDA Class 2 ·Tube, Tracheostomy (W/Wo Connector)

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar