Primary Device ID | 00815671020246 |
NIH Device Record Key | a670efd8-07ba-433d-b1f5-7df7c312b337 |
Commercial Distribution Discontinuation | 2016-09-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Sensei® |
Version Model Number | 08257 |
Catalog Number | 08257 |
Company DUNS | 128941304 |
Company Name | HANSEN MEDICAL, 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 | false |
OTC Over-The-Counter | false |
Phone | 1-650-404-5844 |
xx@xx.xx | |
Phone | 1-650-404-5844 |
xx@xx.xx | |
Phone | 1-650-404-5844 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815671020246 [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 | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-30 |
00815671020260 | Sensei X2 Robotic System 120V |
00815671020246 | Sensei X Robotic System Reconditioned 120V |