Primary Device ID | 04056869039176 |
NIH Device Record Key | 52311c92-4608-4f3c-9c36-c6a7b8ec1fc9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MAGNETOM Vida |
Version Model Number | 11060815 |
Company DUNS | 313217003 |
Company Name | Siemens Healthcare GmbH |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04056869039176 [Primary] |
LNH | System, nuclear magnetic resonance imaging |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-03-24 |
Device Publish Date | 2017-07-25 |
04056869039176 | MRI Scanner |
04056869260143 | MRI Scanner |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MAGNETOM VIDA 79205326 5377429 Live/Registered |
Siemens Healthcare GmbH 2017-01-24 |