FDA device listing

BVI1689 (CH1,EP1) - Retrobulbar,BVI1689 (EP1, CH1) - Peribulbar,Clearside6394 (MN,SP) - SCS Microinjector,Depuy (NR)…

FDA device listing 1446341355 · STERIS Corporation

Key facts

Proprietary names BVI1689 (CH1,EP1) - Retrobulbar,BVI1689 (EP1, CH1) - Peribulbar,Clearside6394 (MN,SP) - SCS Microinjector,Depuy (NR) - CELLECT BONE MARRO; CONFIDENCE SPINAL CEMENT SYSTEM,Merit1383 (NT,SN) - ShortStop Advantage Temporary Sharps Holder,Merit1383 (SN) - ShortStop Advantage Temporary Sharps Holder,Merit1383 (SN) - ShortStop Temporary Sharps Holder,Merit1383 (TM) - BackStop Plus Closed Waste…
Owner/operator STERIS Corporation
Owner/operator number 1527821
Product codes GAA
Device names GAA - Needle, Aspiration And Injection, Disposable
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments Isomedix Operations Inc, Isomedix Operations, Inc, Isomedix Operations, Inc., ISOMEDIX OPERATIONS INC, ISOMEDIX OPERATIONS INC.
Establishment registrations 1047843, 1220477, 1319660, 1424263, 1450662, 1643817, 1720929, 2030624, 2032098, 2183744, 3009888344
FEI numbers 1047843, 1220477, 1450662, 1643817, 1720929, 2183744, 1000136478, 3000206435, 3003015552, 3003058448, 3009888344
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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