| Primary Device ID | 06936415985462 |
| NIH Device Record Key | 39bf0419-ff78-4eb8-b1f2-3c4cf5b2cf2c |
| Commercial Distribution Discontinuation | 2024-12-11 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | BeneVision N12 OR Patient Monitor |
| Version Model Number | BeneVision N12 OR |
| 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 | 06936415985462 [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 | 2024-12-19 |
| Device Publish Date | 2024-12-11 |
| 06936415985462 - BeneVision N12 OR Patient Monitor | 2024-12-19 |
| 06936415985462 - BeneVision N12 OR Patient Monitor | 2024-12-19 |
| 06936415919283 - uMEC6 Patient Monitor | 2024-12-02 |
| 06936415903527 - VS-900c Vital Signs Monitor | 2024-11-28 |
| 06936415980702 - A3 Anesthesia Delivery System | 2024-11-28 |
| 06944904040301 - VS-900 Vital Signs Monitor | 2024-11-28 |
| 06944904097923 - cPM 8 Patient Monitor | 2024-11-28 |
| 06944904097930 - cPM 12 Patient Monitor | 2024-11-28 |
| 06936415927127 - ePM 12MA Patient Monitor | 2024-11-27 |