19 results · 45ms · Sources: EU EUDAMED, US FDA

AG MARKETING & DEVELOPMENT GROUP INC DBA AGMD GROUP

FDA registration
AG MARKETING & DEVELOPMENT GROUP INC DBA AGMD GROUP·3 products·🇨🇦 Canada

Medline Green Ambidextrous PF Nitrile Exam Gloves With Colloidal Oatmeal USP (Tested For Use With Chemotherapy Drugs)

FDA registration
MEDLINE INDUSTRIES, LP - Northfield·3 products·🇺🇸 United States

HARTALEGA SDN BHD

FDA registration
HARTALEGA SDN BHD·3 products·🇲🇾 Malaysia

CBR ENTERPRISE LIMITED

FDA registration
CBR ENTERPRISE LIMITED·3 products·🇭🇰 Hong Kong

HARTALEGA NGC SDN BHD

FDA registration
HARTALEGA NGC SDN BHD·3 products·🇲🇾 Malaysia

Medline Green Ambidextrous Power-Free Nitrile Examination Gloves with Colloidal Oatmeal USP (Tested for Use with Chemotherapy Drugs)

FDA 510(k)
FDA Class 1 ·General Hospital

SURGICAL INSTRUMENT MANUFACTURERS, LLC

FDA registration
SURGICAL INSTRUMENT MANUFACTURERS, LLC·1 product·🇺🇸 United States

VVR 4000i

FDA registration
Steril Verona srl·3 products·🇮🇹 Italy

VVR4000i SMARxT

FDA registration
SORIN GROUP ITALIA S.R.L·3 products·🇮🇹 Italy

PIN SCREW

FDA UDI
BK MEDITECH CO.,LTD.·08809155854917·Wire Pin Screw, 2.3mm Shaft Diameter x 2.3mm Th...

PIN SCREW

FDA UDI
BK MEDITECH CO.,LTD.·08809155854979·Wire Pin Screw, 2.3mm Shaft Diameter x 2.3mm Th...

Quantum Blood and Fluid Warming System

FDA registration
CONTRACT MEDICAL MANUFACTURING, LLC·2 products·🇺🇸 United States

Boston Scientific Corporation

FDA registration
Boston Scientific Corporation·1 product·🇺🇸 United States

ANDERSEN SCIENTIFIC, INC.

FDA registration
ANDERSEN SCIENTIFIC, INC.·1 product·🇺🇸 United States

STAXX XDL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

SORIN VVR 4000I AND 4000I SMARXT FILTERED HARDSHELL VENOUS RESERVOIR

FDA 510(k)
FDA Class 2 ·Cardiovascular

Polymer Patient Examination Glove

FDA classification
FDA Class 1 ·Polymer Patient Examination Glove

Reservoir, Blood, Cardiopulmonary Bypass

FDA classification
FDA Class 2 ·Reservoir, Blood, Cardiopulmonary Bypass

Spinal Vertebral Body Replacement Device

FDA classification
FDA Class 2 ·Spinal Vertebral Body Replacement Device