| Primary Device ID | 06903053000451 |
| NIH Device Record Key | beafb0b3-84b3-4812-811a-e63b6935d984 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BeneVision N17 Neo Patient Monitor |
| Version Model Number | BeneVision N17 Neo |
| Company DUNS | 654671304 |
| Company Name | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06903053000451 [Primary] |
| MHX | Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-03 |
| Device Publish Date | 2025-01-24 |
| 06903053000451 - BeneVision N17 Neo Patient Monitor | 2025-02-03 |
| 06903053000451 - BeneVision N17 Neo Patient Monitor | 2025-02-03 |
| 06903053000468 - BeneVision N15 Neo Patient Monitor | 2025-02-03 |
| 06903053037747 - BeneVision M17C Patient Monitor | 2025-02-03 |
| 06903053037754 - BeneVision M15C Patient Monitor | 2025-02-03 |
| 06903053037761 - BeneVision M12C Patient Monitor | 2025-02-03 |
| 06903053037778 - BeneVision M19C Patient Monitor | 2025-02-03 |
| 06903053037785 - BeneVision M22C Patient Monitor | 2025-02-03 |
| 06903053064453 - BeneVision N22 OR Patient Monitor | 2025-02-03 |