| Primary Device ID | 08430215046203 |
| NIH Device Record Key | f71009f1-0e31-4f72-bf31-521800c37df5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LightCycler® 2.0 Instrument |
| Version Model Number | 03531414001 |
| Catalog Number | 03531414001 |
| Company DUNS | 071674100 |
| Company Name | Roche Molecular Systems, 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 | true |
| 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 | 08430215046203 [Primary] |
| OOI | real time Nucleic acid amplification 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 | 2020-07-07 |
| Device Publish Date | 2014-09-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LIGHTCYCLER 76142721 2756741 Live/Registered |
ROCHE DIAGNOSTICS GMBH 2000-10-09 |
![]() LIGHTCYCLER 75257374 2247017 Live/Registered |
ROCHE DIAGNOSTIC GMBH 1997-03-14 |