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

Keos Lumbar IBFD

FDA registration
KEOS·1 product·🇺🇸 United States

Keos Lumbar IBFD

FDA 510(k)
FDA Class 2 ·Orthopedic

Sterigenics US LLC

FDA registration
Sterigenics US LLC·2 products·🇺🇸 United States

Sterigenics U.S., LLC

FDA registration
Sterigenics U.S., LLC·2 products·🇺🇸 United States

Biograph 64 TruePoint

FDA registration
SIEMENS MEDICAL SOLUTIONS USA, INC.·2 products·🇺🇸 United States

Affinity CP Centrifugal Pump

FDA registration
MEDTRONIC PERFUSION SYSTEMS·2 products·🇺🇸 United States

External Motor

FDA registration
Plexus Manufacturing Sdn. Bhd.·1 product·🇲🇾 Malaysia

AFFINITY CP CENTRIFUGAL BLOOD PUMP

FDA registration
KYOCERA Corporation Shiga Yasu Plant·2 products·🇯🇵 Japan

Affinity CP Centrifugal Pump

FDA registration
Medtronic Mexico S. de R.L. de CV·2 products·🇲🇽 Mexico

Affinity CP Centrifugal Blood Pump

FDA registration
MIDWEST STERILIZATION CORP.·2 products·🇺🇸 United States

Siemens Biograph 64 PET/CT

FDA registration
MEDIVEST GROUP·2 products·🇬🇧 United Kingdom

Biograph 64 TruePoint

FDA registration
SIEMENS MEDICAL SOLUTIONS USA, INC.·2 products·🇺🇸 United States

VENNER MEDICAL (SINGAPORE) PTE LTD

FDA registration
VENNER MEDICAL (SINGAPORE) PTE LTD·1 product·🇸🇬 Singapore

PRIMED LIYANG MEDICAL PRODUCTS MANUFACTURING CO., LTD.

FDA registration
PRIMED LIYANG MEDICAL PRODUCTS MANUFACTURING CO., LTD.·1 product·🇨🇳 China

iLIGHT Ultra Face and Body

FDA registration
Spectrum Brands, Inc. (a Delaware Corporation)·1 product·🇺🇸 United States

Gushi priMED Medical Products Manufacturing Co., Ltd.

FDA registration
Gushi priMED Medical Products Manufacturing Co., Ltd.·1 product·🇨🇳 China

priMED Jiujiang Medical Products Manufacturing Co., Ltd

FDA registration
priMED Jiujiang Medical Products Manufacturing Co., Ltd·1 product·🇨🇳 China

AFFIITY CP CENTRIFUGAL BLOOD PUMP

FDA 510(k)
FDA Class 2 ·Cardiovascular

BIOGRAPH 64 AND BIOGRAPH 40

FDA 510(k)
FDA Class 2 ·Radiology

Intervertebral Fusion Device With Bone Graft, Lumbar

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