FDA device listing
Medline tracheobronchial suction catheter kit
FDA device listing 1553133942 · MIDWEST STERILIZATION CORP.
Key facts
| Proprietary names | Medline tracheobronchial suction catheter kit |
|---|---|
| Owner/operator | MIDWEST STERILIZATION CORP. |
| Owner/operator number | 1928237 |
| Product codes | OFR |
| Device names | OFR - Tracheobronchial Suction Catheter Kit |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.6810 |
| Review panels | Anesthesiology |
| 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