FDA device listing
Medline Gauze Sponge,Micro instrument wipe,Non-sterile micro instrument wipe,Occular Occluder,Ocular occluder,Shah aural…
FDA device listing 1548926696 · MIDWEST STERILIZATION CORP.
Key facts
| Proprietary names | Medline Gauze Sponge,Micro instrument wipe,Non-sterile micro instrument wipe,Occular Occluder,Ocular occluder,Shah aural dressing |
|---|---|
| Owner/operator | MIDWEST STERILIZATION CORP. |
| Owner/operator number | 1928237 |
| Product codes | NAB |
| Device names | NAB - Gauze / Sponge,Nonresorbable For External Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4014 |
| Review panels | General & Plastic Surgery |
| Registered establishments | MIDWEST STERILIZATION CORP. |
| Establishment registrations | 1928237, 3005012805 |
| FEI numbers | 1928237, 3005012805 |
| Establishment operations | Contract Sterilizer |
| 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