21 results · 43ms · Sources: EU EUDAMED, US FDA

Ingenia 3T

FDA registration
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·2 products·🇳🇱 Netherlands

Ingenia 3T

FDA registration
Philips India Limited - Magnetic Resonance Business Unit·2 products·🇮🇳 India

Ingenia 3.0T, Ingenia 3.0T CX, Ingenia Elition and MR 7700 with Distributed Multi Nudclei

FDA 510(k)
FDA Class 2 ·Radiology

XN CHECK BF

FDA UDI
SYSMEX CORPORATION·14987562460318·XN CHECK BF 6X3.0ML L 1,2

Photoplethysmograph Analysis Software For Over-The-Counter Use - Irregular Rhythm Notification Feature (2)

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

YOMURA TECHNOLOGIES INC.

FDA registration
YOMURA TECHNOLOGIES INC.·1 product·🇹🇼 Taiwan

OsteoMed

FDA UDI
OSTEOMED LLC·00845694020305·FPS 3.5mm x 16mm Standard Screw

Vu a-POD™

FDA UDI
SEASPINE ORTHOPEDICS CORPORATION·10889981038229·35x27mm Trial 16mm 12 deg. The Vu a-POD interve...

OsteoMed

FDA UDI
OSTEOMED LLC·00845694074322·FPS 3.5 x 16mm Screw Sterile Qty 2

Life Scope® BSM 6000 Series Bedside Monitoring Systems

FDA registration
NIHON KOHDEN TOMIOKA PRODUCTION CENTER·1 product·🇯🇵 Japan

Axion Stim-Pro I-2000

FDA registration
AXION USA·1 product·🇺🇸 United States

Life Scope® BSM 6000 Series Bedside Monitoring Systems

FDA registration
NIHON KOHDEN AMERICA, INC.·1 product·🇺🇸 United States

DERMABOND™ PRINEO™ Skin Closure System (22cm)

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

Life Scope® BSM 6000 Series Bedside Monitoring Systems

FDA registration
Nihon Kohden Corporation - Eastern Japan Logistics Center·1 product·🇯🇵 Japan

DERMABOND™ PRINEO™ Skin Closure System (22cm)

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

Life Scope® BSM 6000 Series Bedside Monitoring Systems

FDA registration
NIHON KOHDEN CORP.·1 product·🇯🇵 Japan

THERASOM-CAST

FDA 510(k)
FDA Class 2 ·Dental

INVACARE ELEVATING SEAT OPTION ESS6

FDA 510(k)
FDA Class 2 ·Physical Medicine

System, Nuclear Magnetic Resonance Imaging

FDA classification
FDA Class 2 ·System, Nuclear Magnetic Resonance Imaging

Device, Anti-Snoring

FDA classification
FDA Class 2 ·Device, Anti-Snoring