| Primary Device ID | 00630414019789 |
| NIH Device Record Key | 27059857-d8e3-4971-ab7d-8aab1a625868 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ADVIA 2120i with SAA Autosampler |
| Version Model Number | 11219530 |
| Catalog Number | 11219530 |
| Company DUNS | 064608573 |
| Company Name | Siemens Healthcare Diagnostics 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 | 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 | 00630414019789 [Primary] |
| GKZ | Counter, differential cell |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-12-23 |
| Device Publish Date | 2018-03-23 |
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