20 results
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41ms
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Sources: EU EUDAMED, US FDA
Synergy Health Ireland Ltd
FDA registration
Synergy Health Ireland Ltd·1 product·🇮🇪 Ireland
KCI USA, INC.
FDA registration
KCI USA, INC.·1 product·🇺🇸 United States
KCI USA, INC.
FDA registration
KCI USA, INC.·1 product·🇺🇸 United States
KCI Manufacturing
FDA registration
KCI Manufacturing·1 product·🇮🇪 Ireland
Dermatac Drape and V.A.C. Granufoam Dressings Featuring SensaT.R.A.C. Technology-Small (5 pack), Dermatac Drape and V.A.C. Granufoam Dressings Featuring SensaT.R.A.C. Technology -Small (10 pack), Dermatac Drape and V.A.C. Granufoam Dressings Featuring SensaT.R.A.C. Technology - Medium(5 pack), Dermatac Drape and V.A.C. Granufoam Dressings Featuring SensaT.R.A.C. Technology -Medium (10 pack), Dermatac Drape and V.A.C. Granufoam Dressings Featuring SensaT.R.A.C. Technology- Large (5 pac
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CoRoent
FDA UDI
Nuvasive, Inc.·00887517578471·CoRoent Ant TLIF Ti, 11x12x32mm 0°
Negative Pressure Wound Therapy Powered Suction Pump
FDA classification
FDA Class 2
·Negative Pressure Wound Therapy Powered Suction Pump
Health & Life Corporation
FDA registration
Health & Life Corporation·1 product·🇹🇼 Taiwan
POWERPRO TRANSFER BATTERY CASE
FDA registration
Linvatec Corporation d/b/a ConMed Linvatec·1 product·🇺🇸 United States
LIVING SCIENCE CO., LTD.
FDA registration
LIVING SCIENCE CO., LTD.·1 product·🇨🇳 China
HEALTH & LIFE MEDICAL TECHNOLOGY COMPANY LIMITED
FDA registration
HEALTH & LIFE MEDICAL TECHNOLOGY COMPANY LIMITED·1 product·🇻🇳 Vietnam
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0123200·Inserter, Tulips and Connectors
Deltec
FDA UDI
SMITHS MEDICAL MD, INC.·10610586025112·
Catheter, Percutaneous, Neurovasculature
FDA registration
NEURAVI LIMITED·1 product·🇮🇪 Ireland
REF03 ClearCorrect System Aligners (Multi-layer)
FDA registration
etkon GMBH·1 product·🇩🇪 Germany
NaturaLyte Liquid Acid Concentrate
FDA registration
Haemotec, a division of Fresenius Medical Care Canada Inc.·1 product·🇨🇦 Canada
FULL AUTOMATIC (NIBP) BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
POWERPRO BATTERY SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Saw, Powered, And Accessories
FDA classification
FDA Class 1
·Saw, Powered, And Accessories
System, Measurement, Blood-Pressure, Non-Invasive
FDA classification
FDA Class 2
·System, Measurement, Blood-Pressure, Non-Invasive