| Primary Device ID | 04931921004708 |
| NIH Device Record Key | af8e7590-b004-4b82-98d6-19c960ad21b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nihon Kohden Life Scope G7 Bedside Monitoring System |
| Version Model Number | QM-151P |
| Catalog Number | QM-151P |
| Company DUNS | 690568050 |
| Company Name | NIHON KOHDEN CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04931921004708 [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 | 2021-10-05 |
| Device Publish Date | 2021-09-27 |
| 04931921023631 | Battery pack (for CU-171R, CU-172R) |
| 04931921006689 | Software Kit (for CU-171R, CU-172R) |
| 04931921004791 | Wall mount kit (for CU-171R, CU-172R) |
| 04931921004784 | Stand (for CU-171R, CU-172R) |
| 04931921004777 | Cart (for CU-171R, CU-172R) |
| 04931921004708 | SD card (for CU-171R, CU-172R) |
| 04931921004692 | Rear option board (for CU-171R, CU-172R) |
| 04931921004661 | Recorder module (for CU-171R, CU-172R) |
| 04931921004593 | Data acquisition unit (for CU-171R, CU-172R) |
| 04931921004555 | Core unit |
| 04931921004517 | Core unit |