Primary Device ID | 04056869297286 |
NIH Device Record Key | 93d65ca7-d518-44d2-ae55-da234803b981 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AI-Rad Companion (Cardiovascular) |
Version Model Number | 11583324 |
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 | false |
Manufacturing Date | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04056869297286 [Primary] |
JAK | System, x-ray, tomography, computed |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-20 |
Device Publish Date | 2023-03-10 |
04056869251226 | 11270037 |
04056869297286 | 11583324 |