FDA device listing

Manifold, Stopcock, and Adapter,MEDLINE ADAPTOR, STOPCOCK, MANIFOLD, FITTING, CARDIOPULMONARY BYPASS,Medline M/M…

FDA device listing 1895787600 · Medline Industries, LP

Key facts

Proprietary names Manifold, Stopcock, and Adapter,MEDLINE ADAPTOR, STOPCOCK, MANIFOLD, FITTING, CARDIOPULMONARY BYPASS,Medline M/M Adapter,NAMIC 3-Way Stopcock,NAMIC Adaptors/Connectors,Push Style Y-Adapter
Owner/operator Medline Industries, LP
Owner/operator number 1417592
Product codes DTL
Device names DTL - Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Device class Class II
Classification regulations (21 CFR) 870.4290
Review panels Cardiovascular
Registered establishments MEDLINE INDUSTRIES, LP - Laredo, Medline Industries, LP - Mexicali (MXC), MEDLINE INDUSTRIES, LP - Northfield, MEDLINE INDUSTRIES, LP (Northpoint Services), MEDLINE INDUSTRIES, LP - SPT, Medline Industries (NAMIC Division) - Glen Falls, Medline Soluciones Medicas, Nuevo Laredo Directo al Cliente, PRODUCTOS MEDLINE S.A. DE C.V.
Establishment registrations 1417592, 1422634, 1423395, 3004122598, 3005595283, 3015173212, 3015910259, 3045816902, 3045816907
FEI numbers 1417592, 1000514656, 3000717925, 3004122598, 3005595283, 3015173212, 3015910259, 3045816902, 3045816907
Establishment operations Contract Sterilizer, Manufacturer, Repackager/Relabeler, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed 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

Browse all FDA device listings