QUADROX-i Neonatal Micorporous Membrane Oxygenator with and without integrated Arterial Filter with SOFTLINE Coating or

FDA registration

Sterigenics Belgium Petit Rechain S.A.·3 products·🇧🇪 Belgium

QUADROX-I NEONATAL MICROPOROUS MEMBRANE OXYGENATOR WITH INTEGRATED ARTERIAL FILTER WITH SOFTLINE/BIOLINE COATING

FDA 510(k)

FDA Class 2 ·Cardiovascular

Blade Scalpel

FDA UDI

KATENA PRODUCTS, INC.·00841668113479·MINIATURE BLADE #64 (BX/5)

Dornhoffer Ti PORP

FDA registration

GYRUS ACMI, INC.·1 product·🇺🇸 United States

Dornhoffer Ti PORP

FDA registration

GYRUS ACMI, INC.·1 product·🇺🇸 United States

Dornhoffer ti porp 2mm

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

Dornhoffer Ti PORP

FDA registration

Gyrus ACMI, Inc.·1 product·🇺🇸 United States

HUMAN MED AG

FDA registration

HUMAN MED AG·1 product·🇩🇪 Germany

Oxygenator, Cardiopulmonary Bypass

FDA classification

FDA Class 2 ·Oxygenator, Cardiopulmonary Bypass

Portex

FDA UDI

Smiths Medical ASD, Inc.·15019517071399·

Eu-tTG IgG

FDA registration

EUROSPITAL S.P.A.·1 product·🇮🇹 Italy

uTASWako AFP-L3 Control L and H

FDA registration

FUJIFILM Wako Pure Chemical Corporation Diagnostics Design Office (Amagasaki)·5 products·🇯🇵 Japan

Patient Vinyl Examination Gloves, Powder Free, Non-Sterile

FDA registration

ZIBO YINGBO MEDICAL PRODUCTS CO., LTD.·1 product·🇨🇳 China

uTASWako AFP-L3 Control L and H

FDA registration

FUJIFILM Healthcare Manufacturing Corporation MIE Office·5 products·🇯🇵 Japan

FUJIFILM Healthcare Americas Corporation

FDA registration

FUJIFILM Healthcare Americas Corporation·5 products·🇺🇸 United States

FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Takematsu Office

FDA registration

FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Takematsu Office·5 products·🇯🇵 Japan

SMITH & NEPHEW OFF-CENTERED PORP

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

HELIX HYDRO-JET

FDA 510(k)

FDA Class 2 ·General Hospital

Lavage, Jet

FDA classification

FDA Class 2 ·Lavage, Jet

Prosthesis, Partial Ossicular Replacement

FDA classification

FDA Class 2 ·Prosthesis, Partial Ossicular Replacement