FDA device listing

0210-010-000,0210-010-100,0210-010-100S1,0210-012-000,0210-014-000,0210-014-100,0210-014-600,0210-015-000,0210-016-000,0…

FDA device listing 1425814181 · Sotera Health LLC

Key facts

Proprietary names 0210-010-000,0210-010-100,0210-010-100S1,0210-012-000,0210-014-000,0210-014-100,0210-014-600,0210-015-000,0210-016-000,0210-018-000,0210-018-100,0210-018-200,0210-058-000,0210-100-000,0210-100-000S4,0210-110-000,0210-110-100,0210-112-000,0210-114-000,0210-114-000S5,0210-114-100,0210-114-100S1,0210-118-000,0210-118-100,0210-118-200,0210-158-000,0210-165-000,0210-166-000,0210-167-000,0210-200-000,02…
Owner/operator Sotera Health LLC
Owner/operator number 10029425
Product codes FQH
Device names FQH - Lavage, Jet
Device class Class II
Classification regulations (21 CFR) 880.5475
Review panels General Hospital
Registered establishments Sterigenics Belgium (Petit Rechain) SRL, Sterigenics SAS, Sterigenics U.S. LLC, Sterigenics U.S., LLC, Sterigenics US LLC, Sterigenics US, LLC
Establishment registrations 1036836, 1054811, 1058584, 1423662, 1526534, 1649518, 2011171, 2029275, 3002907620, 3005941719, 3007156625
FEI numbers 1036836, 1526534, 2011171, 1000114185, 1000219637, 1000306431, 3000215273, 3001236277, 3002807111, 3002907620, 3008133910
Establishment operations Contract Sterilizer
Registration valid through 2026

At a glance

  • 10–99 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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