14 results
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41ms
·
Sources: EU EUDAMED, US FDA
Peridot-EX Expandable Intervertebral body fusion system
FDA registration
GBS COMMONWEALTH, CO. LTD.·1 product·🇰🇷 South Korea
Peridot-EX Expandable Intervertebral Body Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
myAirvo 3
FDA registration
FISHER & PAYKEL HEALTHCARE, INC.·1 product·🇺🇸 United States
myAirvo 3
FDA registration
FISHER & PAYKEL HEALTHCARE, LTD.·1 product·🇳🇿 New Zealand
Biotornix Healthcare AV Safety Fistula Needle
FDA registration
BIOTRONIX HEALTHCARE INDUSTRIES INC.·2 products·🇺🇸 United States
LAA Exclusion System
FDA registration
CELESTICA de MONTERREY S.A. de C.V.·1 product·🇲🇽 Mexico
LAA Exclusion System
FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States
Versa PRO
FDA registration
VENUS CONCEPT INC.·3 products·🇺🇸 United States
LAA Exclusion System
FDA registration
MEDTRONIC PERFUSION SYSTEMS·1 product·🇺🇸 United States
UDE
FDA 510(k)
FDA Class 2
·Radiology
BIOTEQUE A.V. FISTULA NEEDLE SET WITH SAFETY FLEX
FDA 510(k)
FDA Class 2
·General Hospital
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
FDA classification
FDA Class 2
·Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
System, Image Processing, Radiological
FDA classification
FDA Class 2
·System, Image Processing, Radiological