FDA device listing
BAM Air LC Repositioning Sheet,BAM Air LC System
FDA device listing 1311434109 · EHOB, INC.
Key facts
| Proprietary names | BAM Air LC Repositioning Sheet,BAM Air LC System |
|---|---|
| Owner/operator | EHOB, INC. |
| Owner/operator number | 1832066 |
| Product codes | FSA |
| Device names | FSA - Lift, Patient, Non-Ac-Powered |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.5510 |
| Review panels | General Hospital |
| Registered establishments | EHOB Distribution Center W. 21st Street, EHOB, INC., EHOB(JiaXing) Medical Product Co., LTD., EHOB (Shanghai) Medical Products Co. Ltd., Shanghai EHOB Health Care Products Co., LTD. |
| Establishment registrations | 1832066, 3012643605, 3018117722, 3020225550, 3024761165 |
| FEI numbers | 1832066, 3012643605, 3018117722, 3020225550, 3024761165 |
| Establishment operations | Complaint File Establishment, Contract Manufacturer, Repackager/Relabeler |
| 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