22 results · 42ms · Sources: EU EUDAMED, US FDA

ACUSON Sequoia Diagnostic Ultrasound System

FDA registration
SIEMENS MEDICAL SOLUTIONS USA, INC.·4 products·🇺🇸 United States

ACUSON Sequoia Diagnostic Ultrasound System

FDA registration
Siemens Healthineers Ltd.·4 products·🇰🇷 South Korea

CW2; CW5

FDA registration
TRANSDUCERWORKS·1 product·🇺🇸 United States

KONICA MINOLTA TECHNOPRODUCTS CO., LTD.

FDA registration
KONICA MINOLTA TECHNOPRODUCTS CO., LTD.·1 product·🇯🇵 Japan

ACUSON Sequoia Diagnostic Ultrasound System

FDA 510(k)
FDA Class 2 ·Radiology

16M - Puget Sound Energy - Metal

FDA UDI
Certified Safety Manufacturing, Inc.·00766588014692·16M - Puget Sound Energy - Metal

16PW - Washington Gas - Poly White

FDA UDI
Certified Safety Manufacturing, Inc.·00766588014425·16PW - Washington Gas - Poly White

EtchPro Etching Gel

FDA registration
PAC-DENT INC.·1 product·🇺🇸 United States

Sterigenics U.S., LLC

FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States

RediGuard® Intra-Aortic Balloon Catheter

FDA registration
Arrow Internacional de Chihuahua S.A. de C.V.·1 product·🇲🇽 Mexico

The Belport Company, Inc DBA Gingi-Pak

FDA registration
The Belport Company, Inc DBA Gingi-Pak·1 product·🇺🇸 United States

RediGuard® Intra-Aortic Balloon Catheter

FDA registration
Arrow International, LLC (subsidiary of Teleflex, Incorporated)·1 product·🇺🇸 United States

BEGO IMPLANT SYSTEMS GMBH & CO. KG

FDA registration
BEGO IMPLANT SYSTEMS GMBH & CO. KG·1 product·🇩🇪 Germany

CD Horizon™ Spinal System

FDA registration
Sterigenics US, LLC·7 products·🇺🇸 United States

Arisure Closed System Drug Transfer Device (CSTD)

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

Integra®

FDA UDI
INTEGRA PAIN MANAGEMENT·10381780429722·Epidural Tray, 18G

Integra®

FDA UDI
INTEGRA PAIN MANAGEMENT·10381780260578·EPIDURAL TRAY, 18G

CARESIDE HEMOGLOBIN

FDA 510(k)
FDA Class 2 ·Hematology

ARROW INTRA-AORTIC BALLOON (IAB) CATHETER WITH A FIBER OPTIC SENSOR AND A MEASUREMENT SYSTEM, MODELS IAB-05830-F,IAB5840

FDA 510(k)
FDA Class 2 ·Cardiovascular

Whole Blood Hemoglobin Determination

FDA classification
FDA Class 2 ·Whole Blood Hemoglobin Determination