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)