10,000 results · 709ms · Sources: EU EUDAMED, US FDA

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Table, Mechanical

FDA classification
FDA Class 1 ·Table, Mechanical

GNW / ANTISERA, CF, INFLUENZA VIRUS A, B, C

FDA registration
MONOCENT INC.·1 product·🇺🇸 United States

SARL CICRETES

Manufacturer
🇩🇿 Algeria·8 Basic UDI-DIs·15 Devices·1 Importer

TriVirum, Inc.

Manufacturer
🇺🇸 United States

Tripollar Device

FDA registration
Passiflora inc.·1 product·🇺🇸 United States

Tripollar Device

FDA registration
Passiflora inc.·1 product·🇺🇸 United States

In2 Patch

FDA registration
Passiflora inc.·1 product·🇺🇸 United States

Zutta LED Mask

FDA registration
Passiflora inc.·3 products·🇺🇸 United States

Resona I8W, Resona I8, Resona I8 Exp, Resona I8S, Resona I8T, Resona IY, Resona I8 Easi Diagnostic Ultrasound System

FDA registration
Shenzhen Mindray Bio-Medical Electronics Co.,LTD·3 products·🇨🇳 China

Resona I8W, Resona I8, Resona I8 Exp, Resona I8S, Resona I8T, Resona IY, Resona I8 Easi Diagnostic Ultrasound System

FDA registration
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD.·3 products·🇨🇳 China

ePlex Respiratory Pathogen (RP) Panel

FDA registration
GENMARK DIAGNOSTICS, INC.·10 products·🇺🇸 United States

cobas® eplex blood culture identification fungal pathogen (BCID-FP) panel

FDA registration
GENMARK DIAGNOSTICS, INC.·3 products·🇺🇸 United States

GenMark ePlex Instrument

FDA registration
GENMARK DIAGNOSTICS, INC.·1 product·🇺🇸 United States

Pre-Sure

FDA registration
LAZARUS 3D, INC.·1 product·🇺🇸 United States

ePlex Blood Culture Identification Panel - Gram Positive (BCID-GP) Panel

FDA registration
GENMARK DIAGNOSTICS, INC.·3 products·🇺🇸 United States

ePlex SARS-CoV-2 Test

FDA registration
GENMARK DIAGNOSTICS, INC.·1 product·🇺🇸 United States

ePlex Blood Culture Identification Gram Negative (BCID-GN) Panel

FDA registration
GENMARK DIAGNOSTICS, INC.·3 products·🇺🇸 United States

Pre-Sure

FDA registration
LAZARUS 3D, INC.·1 product·🇺🇸 United States

icONE

FDA registration
AB DIGIHEALTH·1 product·🇺🇸 United States

6895-1301 - ADANTE SUPINE TRUNK PAD

FDA registration
MIZUHO ORTHOPEDIC SYSTEMS, INC.·1 product·🇺🇸 United States