Basic Respitrace System

FDA registration

AMBULATORY MONITORING, INC.·1 product·🇺🇸 United States

RESPITRACE

FDA 510(k)

FDA Class 2 ·Anesthesiology

Spirometer, Monitoring (W/Wo Alarm)

FDA classification

FDA Class 2 ·Spirometer, Monitoring (W/Wo Alarm)

CoRoent

FDA UDI

Nuvasive, Inc.·00887517821898·Interlock II Trial, 16x17x14mm 10° Stop

Disposable EEG Cup Electrode

FDA registration

TECHNOMED EUROPE·1 product·🇳🇱 Netherlands

Rochester

FDA registration

Advantage Medical Electronics, LLC, dba AMC·1 product·🇺🇸 United States

Fiber-Connect

FDA registration

Dunamis Medical LLC·1 product·🇺🇸 United States

Fiber-Connect

FDA registration

JANCO, INC.·1 product·🇺🇸 United States

Force Fiber Fusion

FDA registration

Teleflex Medical LLC·1 product·🇺🇸 United States

Force Fiber Fusion

FDA registration

Teleflex Medical LLC·1 product·🇺🇸 United States

Disposable EEG Cup Electrode

FDA registration

TECHNOMED ASIA, PT.·1 product·🇮🇩 Indonesia

Force Fiber Fusion

FDA registration

Teleflex Medical de Mexico, S. de R.L. de C.V.·1 product·🇲🇽 Mexico

Force Fiber Fusion Suture

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

CUP ELECTRODES, GOLD, REUSABLE, SILVER, REUSABLE; CUP ELECTRODES SILVER/SILVER CHLORIDE REUSABLE

FDA 510(k)

FDA Class 2 ·Neurology

Suture, Nonabsorbable, Synthetic, Polyethylene

FDA classification

FDA Class 2 ·Suture, Nonabsorbable, Synthetic, Polyethylene

Electrode, Cutaneous

FDA classification

FDA Class 2 ·Electrode, Cutaneous