21 results · 45ms · Sources: EU EUDAMED, US FDA

NEOSS, LTD.

FDA registration
NEOSS, LTD.·1 product·🇬🇧 United Kingdom

WESLEY COE (CAMBRIDGE) LTD

FDA registration
WESLEY COE (CAMBRIDGE) LTD·1 product·🇬🇧 United Kingdom

NEOSS AB

FDA registration
NEOSS AB·1 product·🇸🇪 Sweden

ELOS MEDTECH TIMMERSDALA AB

FDA registration
ELOS MEDTECH TIMMERSDALA AB·1 product·🇸🇪 Sweden

Neoss Proactive Implant

FDA registration
Swann-Morton(Services) Limited·1 product·🇬🇧 United Kingdom

NEOSS PROACTIVE IMPLANT

FDA 510(k)
FDA Class 2 ·Dental

GE Lightspeed 16 CT scanner

FDA registration
BAY SHORE MEDICAL EQUIPMENT, LLC·1 product·🇺🇸 United States

Fuji CR-IR

FDA registration
CANUTE INTERNATIONAL MEDICAL SERVICES (CANADA) INC·1 product·🇨🇦 Canada

Toyo Medical Co

FDA registration
TOYO MEDICAL CO.·1 product·🇺🇸 United States

LightSpeed Ultra 16

FDA registration
GE HANGWEI MEDICAL SYSTEMS CO., LTD.·1 product·🇨🇳 China

SANICURE BV

FDA registration
SANICURE BV·1 product·🇳🇱 Netherlands

Cassette

FDA registration
FUJIFILM CORPORATION·1 product·🇯🇵 Japan

Cassette

FDA registration
FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Takematsu Office·1 product·🇯🇵 Japan

Titan

FDA registration
MAICO Diagnostics GmbH·1 product·🇩🇪 Germany

SYNERGY HEALTH STERILISATION UK LTD

FDA registration
SYNERGY HEALTH STERILISATION UK LTD·1 product·🇬🇧 United Kingdom

LiquiBand

FDA registration
Sterigenics UK Limited·1 product·🇬🇧 United Kingdom

INVACARE PASSOVER HUMIDIFIER MODEL ISP9700

FDA 510(k)
FDA Class 2 ·Anesthesiology

LIGHTSPEED 4.0 CT SCANNER SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

Implant, Endosseous, Root-Form

FDA classification
FDA Class 2 ·Implant, Endosseous, Root-Form

Humidifier, Respiratory Gas, (Direct Patient Interface)

FDA classification
FDA Class 2 ·Humidifier, Respiratory Gas, (Direct Patient Interface)