cuff

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Contec Medical Systems Co., Ltd.·1 device

George King Congential Factor Deficiency Convenience Kit

FDA UDI

GEORGE KING BIO-MEDICAL, INC·00815696021037·George King CFD is a Congenital Factor Deficien...

Powder-Free Polyisoprene Sterile Surgical Gloves in White Color Tested for Use with Chemotherapy Drugs, Powder-Free Polyisoprene Sterile Surgical Gloves in Green Color.

FDA 510(k)

FDA Class 1 ·General, Plastic Surgery

Polychloroprene Powder-free Surgical Glove (White) Tested for Use with Chemotherapy Drugs; Polychloroprene Powder-free Surgical Glove (Green) Tested for Use with Chemotherapy Drugs

FDA 510(k)

FDA Class 1 ·General, Plastic Surgery

Polychloroprene Powder Free Sterile Surgical Gloves, Low Dermatitis Potential and Tested for Use with Chemotherapy Drugs

FDA 510(k)

FDA Class 1 ·General, Plastic Surgery

Polychloroprene Powder Free Sterile Surgical Gloves, White, Tested for Use with Chemotherapy Drugs

FDA 510(k)

FDA Class 1 ·General, Plastic Surgery

NA

FDA UDI

ECOTRON·08800019200093·1. Line Voltage: 220~230V, 50/60Hz 2. Output Po...

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

System, Endovascular Graft, Aortic Aneurysm Treatment

FDA Pre-Market Approval

FDA Class 3 ·OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM, OVATION IX ILIAC STENT GRAFT

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

Polychloroprene Powder Free Sterile Surgical Gloves, White, Tested for Use with Chemotherapy

FDA 510(k)

FDA Class 1 ·General, Plastic Surgery

CE-2220-PI

Basic UDI-DI

EU MDR · Eu Md Class 1 ·MOBERCAS SL·1 device

EndoPilot

FDA registration

SCHLUMBOHM GMBH & CO. KG·4 products·🇩🇪 Germany

EndoPilot²

FDA registration

GEBR. BRASSELER GMBH & CO. KG·4 products·🇩🇪 Germany

Medical Monitor

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Xuzhou AKX Electronic Science and Technology co.，Ltd·1 device

Digital Electronic Colposcope

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Xuzhou AKX Electronic Science and Technology co.，Ltd·2 devices