RESMED CORP

FDA registration

RESMED CORP·1 product·🇺🇸 United States

RESMED PTY LTD.

FDA registration

RESMED PTY LTD.·1 product·🇦🇺 Australia

MIRAGE FULL FACE MASK SERIES 2

FDA 510(k)

FDA Class 2 ·Anesthesiology

N.A.

FDA UDI

DENTAURUM GmbH & Co.KG·J011023287000·Screw for ligator (REF 023-284-00)

N.A.

FDA UDI

DENTAURUM GmbH & Co.KG·J011023286000·Tip for ligator (REF 023-284-00)

N.A.

FDA UDI

DENTAURUM GmbH & Co.KG·J011023285000·Spool for ligator (REF 023-284-00)

GE, 1.5T HD, 8-Channel, Quad Extremity Coil

FDA registration

Philips Electronics Ltd·1 product·🇨🇦 Canada

GE, 1.5T HD, 8-Channel, Quad Extremity Coil

FDA registration

Philips Global Business Services LLP·1 product·🇮🇳 India

1300 XSBP Xenon Light Source

FDA registration

Medical Illumination International, Inc·1 product·🇺🇸 United States

GE, 1.5T HD, 8-Channel, Quad Extremity Coil

FDA registration

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·1 product·🇳🇱 Netherlands

N.A.

FDA UDI

DENTAURUM GmbH & Co.KG·J011023284000·Ligator

Vilex, Inc.

FDA registration

MEDICAL DEVICE AND IMPLANTS LLC·1 product·🇺🇸 United States

PIEZOSURGERY MEDICAL

FDA registration

MECTRON S.P.A.·5 products·🇮🇹 Italy

LUMEND FRONTRUNNER CTO CORONARY CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

PHLEBOPUMP, MODEL 1000

FDA 510(k)

FDA Class 2 ·Cardiovascular

Ventilator, Non-Continuous (Respirator)

FDA classification

FDA Class 2 ·Ventilator, Non-Continuous (Respirator)

Sleeve, Limb, Compressible

FDA classification

FDA Class 2 ·Sleeve, Limb, Compressible

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous