20 results · 52ms · Sources: EU EUDAMED, US FDA

CYF-V2R

FDA registration
OLYMPUS MEDICAL SYSTEMS CORP.·1 product·🇯🇵 Japan

CYF-V2R

FDA registration
SHIRAKAWA OLYMPUS CO., LTD.·1 product·🇯🇵 Japan

IAN JAMIESON PTY LTD

FDA registration
IAN JAMIESON PTY LTD·1 product·🇦🇺 Australia

CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-V2), CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-V2R), CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-VH) and CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-VHR)

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Cystoscope And Accessories, Flexible/Rigid

FDA classification
FDA Class 2 ·Cystoscope And Accessories, Flexible/Rigid

BD BBL™ Phenol Red Broth with Inositol and Durham Tube

FDA UDI
BECTON, DICKINSON AND COMPANY·30382902216835·BD BBL™ Phenol Red Broth with Inositol and Durh...

ArgenPMMA MQC

FDA registration
THE ARGEN CORPORATION·3 products·🇺🇸 United States

PMMA BLOCK

FDA registration
Shandong Huge Dental Material Corporation·3 products·🇨🇳 China

Sterigenics U.S. LLC

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

Myoaligner Appliance

FDA registration
MYOHEALTH TECHNOLOGIES, LLC·3 products·🇺🇸 United States

BioTemps NOW Milling Block;Bridge Block;A3.5 (5-pack)

FDA registration
PRISMATIK DENTALCRAFT, INC.·3 products·🇺🇸 United States

ArgenPMMA MQC

FDA registration
The Argen Corporation·3 products·🇺🇸 United States

Jabil Circuit (Singapore) Pte Ltd

FDA registration
Jabil Circuit (Singapore) Pte Ltd·1 product·🇸🇬 Singapore

CARDINAL HEALTH D.R. 203 II LTD

FDA registration
CARDINAL HEALTH D.R. 203 II LTD·1 product·🇩🇴 Dominican Republic

NovoSorb MTX

FDA registration
POLYNOVO BIOMATERIALS PTY LTD·1 product·🇦🇺 Australia

IMPERIAL TRADING LIMITED

FDA registration
IMPERIAL TRADING LIMITED·1 product·🇧🇧 Barbados

CINESCAN S

FDA 510(k)
FDA Class 2 ·Radiology

ACCULIF TL CAGE

FDA 510(k)
FDA Class 2 ·Orthopedic

System, Imaging, Pulsed Echo, Ultrasonic

FDA classification
FDA Class 2 ·System, Imaging, Pulsed Echo, Ultrasonic

Intervertebral Fusion Device With Bone Graft, Lumbar

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