FDA device listing

Angio-SAC Collection System,NAMIC Angiographic Bags

FDA device listing 1569487055 · Medline Industries, LP

Key facts

Proprietary names Angio-SAC Collection System,NAMIC Angiographic Bags
Owner/operator Medline Industries, LP
Owner/operator number 1417592
Premarket submissions K843726
Product codes DQO
Device names DQO - Catheter, Intravascular, Diagnostic
Device class Class II
Classification regulations (21 CFR) 870.1200
Review panels Cardiovascular
Registered establishments Medline Industries, LP - Mexicali (MXC), MEDLINE INDUSTRIES, LP (Northpoint Services), Medline Industries (NAMIC Division) - Glen Falls, Nuevo Laredo Directo al Cliente, PRODUCTOS MEDLINE S.A. DE C.V., RCI HUDSON DE MEXICO S. DE RL. DE CV.
Establishment registrations 1422634, 3004122598, 3015173212, 3015910259, 3029706818, 3045816907
FEI numbers 1000514656, 3004122598, 3015173212, 3015910259, 3029706818, 3045816907
Establishment operations Contract Sterilizer, Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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