Primary Device ID | 04056869006734 |
NIH Device Record Key | 676897c1-34e0-486b-8a13-926d8cd8ead2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MAGNETOM Prisma |
Version Model Number | 10849583 |
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 | 04056869006734 [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 | 4 |
Public Version Date | 2020-02-07 |
Device Publish Date | 2016-09-24 |
04056869006734 | MRI Scanner |
04056869006727 | MRI Scanner |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MAGNETOM PRISMA 79125087 4378283 Live/Registered |
Siemens Healthcare GmbH 2012-11-14 |