| Primary Device ID | 04057834082913 |
| NIH Device Record Key | 44c0c2e5-a7bf-4492-84f2-3ca3f01145bf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NEUROVENT-TEMP-IFD-R |
| Version Model Number | 095327-003 |
| Company DUNS | 332785323 |
| Company Name | RAUMEDIC AG |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com | |
| Phone | +18886470070 |
| neuromonitoring@raumedic.com |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Outer Diameter | 3.1 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04057834082913 [Primary] |
| GWM | Device, monitoring, intracranial pressure |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-15 |
| Device Publish Date | 2025-12-05 |
| 04057834029376 | 095327-002 |
| 04057834082913 | 095327-003 |