FDA device listing
URO TRAY REPLACEMENT HOSE FLEX TYPE (10 PER BAG)
FDA device listing 2072609406 · Skytron, LLC
Key facts
| Proprietary names | URO TRAY REPLACEMENT HOSE FLEX TYPE (10 PER BAG) |
|---|---|
| Owner/operator | Skytron, LLC |
| Owner/operator number | 9918015 |
| Product codes | NNW |
| Device names | NNW - Bag, Urine Collection, Leg, For External Use, Non-Sterile |
| Device class | Class I |
| Classification regulations (21 CFR) | 876.5250 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | Skytron, LLC |
| Establishment registrations | 1825014 |
| FEI numbers | 1825014 |
| Establishment operations | Complaint File Establishment |
| 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