FDA device listing
D850 Transfer Board,Schure Slide Ambulance, Full Size,Schure Slide, Anti-Static,Schure Slide, Anti-Static, Rigid,Schure…
FDA device listing 1285121777 · SCHUERCH CORPORATION
Key facts
| Proprietary names | D850 Transfer Board,Schure Slide Ambulance, Full Size,Schure Slide, Anti-Static,Schure Slide, Anti-Static, Rigid,Schure Slide, Ergo,Schure Slide Fts, Long,Schure Slide Fts, Short,Schure Slide, Full Size,Schure Slide, Full Size, Anti-Static, Rigid, Black,Schure Slide, Rigid,Schure Slide Xl,Schure Slide Xla Ambulance,Schure Slide Xlt,Transfer Board With Safety Notches |
|---|---|
| Owner/operator | SCHUERCH CORPORATION |
| Owner/operator number | 10028067 |
| Product codes | FMR |
| Device names | FMR - Device, Transfer, Patient, Manual |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6785 |
| Review panels | General Hospital |
| Registered establishments | SCHUERCH CORPORATION |
| Establishment registrations | 1223962 |
| FEI numbers | 1000305774 |
| Establishment operations | Manufacturer |
| 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