| Primary Device ID | 00840828192668 |
| NIH Device Record Key | 8ecca945-eabd-483f-b0ac-aacf12b8e2b8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REGO HUB,HILLROM NAVICARE,NO-NC,NO-P |
| Version Model Number | HB01-33101101000 |
| Catalog Number | 26178 |
| Company DUNS | 796452311 |
| Company Name | CURBELL MEDICAL PRODUCTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| 00840828192682 - REGO HUB,HILLROM NAVICARE,NO-NC,NO-P,ALT | 2024-07-30 REGO HUB,HILLROM NAVICARE,NO-NC,NO-P,ALT |
| 00840828192699 - REGO HUB,ASCOM TELLIGENCE,NO-NC,NO-P | 2024-07-30 REGO HUB,ASCOM TELLIGENCE,NO-NC,NO-P |
| 00840828192705 - REGO HUB,ASCOM NU,9FT-NO-PWR,RELAYS | 2024-07-30 REGO HUB,ASCOM NU,9FT-NO-PWR,RELAYS |
| 00840828192712 - UNDER BED LIGHT CONTROLLER ASSEMBLY | 2024-07-30 UNDER BED LIGHT CONTROLLER ASSEMBLY |
| 00840828192729 - RESPONDER 5, INTERACTIVE | 2024-07-30 RESPONDER 5, INTERACTIVE |
| 00840828192736 - GEN4 PLUS, DIRECT ACCESS | 2024-07-30 GEN4 PLUS, DIRECT ACCESS |
| 00840828192743 - GEN4 INTERACTIVE | 2024-07-30 GEN4 INTERACTIVE |
| 00840828192750 - GEN4 PLUS, RESPONDER 5, ENHANCED | 2024-07-30 GEN4 PLUS, RESPONDER 5, ENHANCED |