MX40 Release B7

FDA registration

Philips North America LLC·8 products·🇺🇸 United States

MX40 Release B7

FDA registration

Philips Electronics Ltd·8 products·🇨🇦 Canada

MX40 Release B7

FDA registration

Philips North America LLC·8 products·🇺🇸 United States

MX40 Release B.07

FDA 510(k)

FDA Class 2 ·Cardiovascular

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04049772814237·GENUMEDI PT SILVER L VI

Novo Surgical Inc.

FDA UDI

NOVO SURGICAL, INC.·00842331186790·tissue forceps, standard pattern, serrated hand...

HydroFill (Formerly HydroSoft Plus)

FDA registration

MicroVention, Inc.·1 product·🇺🇸 United States

HydroFill (Formerly HydroSoft Plus)

FDA registration

MicroVention Costa Rica S.R.L.·1 product·🇨🇷 Costa Rica

Synergy Health AST, LLC

FDA registration

Synergy Health AST, LLC·1 product·🇺🇸 United States

ATOM MEDICAL CORPORATION

FDA registration

ATOM MEDICAL CORPORATION·1 product·🇯🇵 Japan

TOYO MEDICAL CO.

FDA registration

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

Synergy Health AST, SRL

FDA registration

Synergy Health AST, SRL·1 product·🇨🇷 Costa Rica

HydroFill 10 Advanced

FDA registration

Terumo Medical Canada, Inc.·1 product·🇨🇦 Canada

Xpert Xpress Strep A

FDA registration

CEPHEID AB·1 product·🇸🇪 Sweden

IMPIX SPACER

FDA 510(k)

FDA Class 2 ·Orthopedic

DUAL INCU I

FDA 510(k)

FDA Class 2 ·General Hospital

Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Incubator, Neonatal

FDA classification

FDA Class 2 ·Incubator, Neonatal

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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