| Primary Device ID | 04057834031782 |
| NIH Device Record Key | bc699110-eb4c-4a33-900f-5fee947d02a8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cable DATALOGGER Nihon Kohden |
| Version Model Number | 096006-001 |
| Company DUNS | 332785323 |
| Company Name | RAUMEDIC AG |
| 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 | true |
| 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 | 04057834031782 [Primary] |
| GWM | Device, Monitoring, Intracranial Pressure |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-08-18 |
| 04057834023541 - Tunneling KIT CH8 | 2025-12-16 |
| 04057834090468 - Tunneling KIT CH12 | 2025-12-16 |
| 04057834026115 - NEUROVENT-P | 2025-12-15 |
| 04057834082845 - NEUROVENT | 2025-12-15 |
| 04057834082876 - NEUROVENT-IFD-S | 2025-12-15 |
| 04057834082883 - NEUROVENT-IFD-R | 2025-12-15 |
| 04057834082906 - NEUROVENT-TEMP-IFD-S | 2025-12-15 |
| 04057834082913 - NEUROVENT-TEMP-IFD-R | 2025-12-15 |