FDA device listing

Lysercell WDF,Lysercell WDF II,Lysercell WNR,Lysercell WPC,pocH-pack…

FDA device listing 1580211431 · SYSMEX CORPORATION

Key facts

Proprietary names Lysercell WDF,Lysercell WDF II,Lysercell WNR,Lysercell WPC,pocH-pack L,Stromatolyser-3WP,Stromatolyser-4DL,Stromatolyser-4DS,Stromatolyser-FB,Stromatolyser-IM,Stromatolyser-NR,Stromatolyser-NR(L),Stromatolyser-WH,Sulfolyser,XW pack L
Owner/operator SYSMEX CORPORATION
Owner/operator number 9014170
Product codes GGK
Device names GGK - Products, Red-Cell Lysing Products
Device class Class I
Classification regulations (21 CFR) 864.8540
Review panels Hematology
Registered establishments Sysmex America, Inc., SYSMEX CORPORATION, SYSMEX CORPORATION ONO FACTORY, SYSMEX CORPORATION TECHNO PARK, SYSMEX DO BRASIL IND E COM LTDA, Sysmex Europe SE, SYSMEX REAGENTS AMERICA, INC.
Establishment registrations 9613959, 3005626422, 3006949423, 3008526732, 3009711478, 3010188738, 3010421384
FEI numbers 3002808299, 3002808301, 3005626422, 3006949423, 3008526732, 3009711478, 3010421384
Establishment operations Complaint File Establishment, Contract Manufacturer, Foreign Exporter, Manufacturer, 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

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