19 results · 41ms · Sources: EU EUDAMED, US FDA

BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector

FDA registration
CAREFUSION 2200, INC.·1 product·🇺🇸 United States

BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector

FDA registration
BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·1 product·🇺🇸 United States

BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector

FDA registration
BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. S.A. de C.V.·1 product·🇲🇽 Mexico

BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector

FDA 510(k)
FDA Class 2 ·General Hospital

Intervertebral Fusion Device With Bone Graft, Cervical

FDA registration
Carolina Precision Technologies·1 product·🇺🇸 United States

SURGICAL INSTRUMENT MANUFACTURERS, LLC

FDA registration
SURGICAL INSTRUMENT MANUFACTURERS, LLC·1 product·🇺🇸 United States

CAMBER SPINE COVERIS CERVICAL CAGE

FDA registration
FRIEDRICH DANIELS GMBH·1 product·🇩🇪 Germany

B & G MFG. CO.

FDA registration
B & G MFG. CO.·1 product·🇺🇸 United States

Coveris Cage

FDA registration
CAMBER SPINE TECHNOLOGIES·1 product·🇺🇸 United States

TIE-IN

FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

TIE-IN

FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

Gown

FDA registration
VIET NAM HONG DUC MEDICAL PRODUCTS LIMITED LIABILITY CO.·1 product·🇻🇳 Vietnam

NaviCam Capsule/Tether

FDA registration
ANX ROBOTICA CORP.·2 products·🇺🇸 United States

Tempus ECG-AF

FDA registration
TEMPUS AI, Inc.·1 product·🇺🇸 United States

CAMBER SPINE COVERIS CERVICAL CAGE

FDA 510(k)
FDA Class 2 ·Orthopedic

TIE-IN TRAPEZIUM

FDA 510(k)
FDA Class 2 ·Orthopedic

Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

FDA classification
FDA Class 2 ·Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Prosthesis, Wrist, Carpal Trapezium

FDA classification
FDA Class 2 ·Prosthesis, Wrist, Carpal Trapezium

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification
FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Cervical