7 results
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49ms
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Sources: EU EUDAMED, US FDA
Filters
FDA FEI Number: 3001237338
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LANX FUSION SYSTEM- SA
FDA 510(k)
FDA Class 2
·Orthopedic
Intervertebral Fusion Device With Integrated Fixation, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Integrated Fixation, Lumbar
Philips Fisher & Paykel RT265 Circuit (1141548)
FDA registration
NextPhase Medical Devices LLC·1 product·🇺🇸 United States
DUAL HEATED INFANT VREATHING CIROUITS
FDA 510(k)
FDA Class 2
·Anesthesiology
UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer
FDA classification
FDA Class 2
·Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer
Electrosurgical, Cutting & Coagulation & Accessories
FDA classification
FDA Class 2
·Electrosurgical, Cutting & Coagulation & Accessories