FDA device listing

Hemodialysis Tray (Not A Start/Stop Kit)

FDA device listing 1911359152 · Cardinal Health 200, LLC

Key facts

Owner/operator Cardinal Health 200, LLC
Owner/operator number 9028292
Product codes PPI
Device names PPI - Hemodialysis Tray (Not A Start/Stop Kit)
Device class Class II
Classification regulations (21 CFR) 876.5820
Review panels Gastroenterology & Urology
Registered establishments Cardinal Health 200, LLC, Convertors de Mexico S. de R.L. de C.V
Establishment registrations 1423537, 9616088, 3007329020
FEI numbers 3001236905, 3002902735, 3007329020
Establishment operations Complaint File Establishment, Manufacturer, Repackager/Relabeler
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

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