| Primary Device ID | 10190302005852 |
| NIH Device Record Key | 8271253e-929b-402d-b704-0ede524247a6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ion Torrent |
| Version Model Number | A29362 |
| Company DUNS | 080131636 |
| Company Name | LIFE TECHNOLOGIES CORPORATION |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 10190302005852 [Primary] |
| PQP | Next generation sequencing oncology panel, somatic or germline variant detection system |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2018-06-28 |
| 10190302005852 | A29362 |
| 10190302005845 | A29361 |
| 10190302005821 | A28783 |
| 10190302005814 | A28782 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ION TORRENT 85732075 4898870 Live/Registered |
Life Technologies Corporation 2012-09-18 |
![]() ION TORRENT 85514449 4913922 Live/Registered |
Life Technologies Corporation 2012-01-11 |
![]() ION TORRENT 77890932 4176032 Live/Registered |
LIFE TECHNOLOGIES CORPORATION 2009-12-10 |