| Primary Device ID | 00630414982403 |
| NIH Device Record Key | d6dd5948-dc9b-40fd-b72c-264b2b81949a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IMMULITE® 2000 XPi Sample Nesting Cups |
| Version Model Number | 10374178 |
| Catalog Number | 905288 |
| Company DUNS | 186812384 |
| Company Name | SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS |
| 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 | true |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00630414982403 [Primary] |
| DGC | IGE, ANTIGEN, ANTISERUM, CONTROL |
| JJE | ANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE), FOR CLINICAL USE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 00630414982410 | Test tube, non-sterile |
| 00630414982403 | Test tube, non-sterile |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() IMMULITE 98891511 not registered Live/Pending |
Siemens Healthcare Diagnostics Inc. 2024-12-09 |
![]() IMMULITE 74098401 1653588 Live/Registered |
SIEMENS HEALTHCARE DIAGNOSTICS INC. 1990-09-19 |