Vessel Tip Suppliers
EMAIL INQUIRY to 1 suppliers
Angiodynamics, Inc. | Address: 603 Queensbury Ave, Queensbury, New York 12804, USA 
www.angiodynamics.com | Send Inquiry | Phone: +1-(518)-798-1215, 800-772-6446
FDA Registration: 1056436 Year Established: 1990 Annual Revenues: USD 25-50 Million Employee Count: ~150 Quality: ISO 9001, CE Certified
Products: Angiographic Catheter, Angled Pigtail, Angiographic Catheter Amplatz Left 1.0, Angiographic Catheter, El Gamal Sones, Angiographic Catheter, El Gamal Multipurpose, Anesthetic Infusion Pump (FDA Code: FRN), Angiographic Catheter, ...
Angiodynamics, Inc. provides medical devices for radiologists, surgeons, and other physicians. We offer medical devices for the minimally invasive diagnosis and treatment of cancer and peripheral vasc more...
www.angiodynamics.com | Send Inquiry | Phone: +1-(518)-798-1215, 800-772-6446
FDA Registration: 1056436 Year Established: 1990 Annual Revenues: USD 25-50 Million Employee Count: ~150 Quality: ISO 9001, CE Certified
Products: Angiographic Catheter, Angled Pigtail, Angiographic Catheter Amplatz Left 1.0, Angiographic Catheter, El Gamal Sones, Angiographic Catheter, El Gamal Multipurpose, Anesthetic Infusion Pump (FDA Code: FRN), Angiographic Catheter, ...
Angiodynamics, Inc. provides medical devices for radiologists, surgeons, and other physicians. We offer medical devices for the minimally invasive diagnosis and treatment of cancer and peripheral vasc more...
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EMAIL INQUIRY to 1 Vessel Tip suppliers
FDA Code / Regulation: FKW / 876.5540
A blood access device and accessories is a device intended to provide access to a patient's blood for hemodialysis or other chronic uses. When used in hemodialysis, it is part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and provides access to a patient's blood for hemodialysis. The device includes implanted blood access devices, nonimplanted blood access devices, and accessories for both the implanted and nonimplanted blood access devices.
Classification. (1) Class III (premarket approval) for the implanted blood access device.
