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 |