20 results · 41ms · 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