| Primary Device ID | M58800100230710 |
| NIH Device Record Key | cac6b03b-9f8a-4b13-83b3-7274a6c2a16d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vdrive System |
| Version Model Number | Single Arm |
| Catalog Number | 001-002307-1 |
| Company DUNS | 024942265 |
| Company Name | Stereotaxis, Inc. |
| 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 |
| Phone | 13146786100 |
| info@stereotaxis.com | |
| Phone | 13146786100 |
| info@stereotaxis.com | |
| Phone | 13146786100 |
| info@stereotaxis.com | |
| Phone | 13146786100 |
| info@stereotaxis.com | |
| Phone | 13146786100 |
| info@stereotaxis.com | |
| Phone | 13146786100 |
| info@stereotaxis.com | |
| Phone | 13146786100 |
| info@stereotaxis.com | |
| Phone | 13146786100 |
| info@stereotaxis.com | |
| Phone | 13146786100 |
| info@stereotaxis.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M58800100230710 [Primary] |
| DXX | System, Catheter Control, Steerable |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-07-17 |
| Device Publish Date | 2016-08-01 |
| M58800100230720 | "The Vdrive® system is intended to stabilize, navigate and remotely control: • Compatible In |
| M58800100230710 | "The Vdrive® system is intended to stabilize, navigate and remotely control: • Compatible In |