| Primary Device ID | 00811877010593 |
| NIH Device Record Key | 6ba32db2-dc40-4b6b-8d34-bf34b57b5ecd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ID NOW™ Instrument |
| Version Model Number | EQ00200X |
| Company DUNS | 154148498 |
| Company Name | Alere Scarborough, 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 | true |
| 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 | 00811877010593 [Primary] |
| OOI | Real Time Nucleic Acid Amplification System |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-11-29 |
| Device Publish Date | 2018-10-29 |
| 00811877010616 | The ID NOW™ Instrument is a portable, fluorescence based instrument intended to be used for th |
| 00811877010593 | The ID NOW™ Instrument is a portable, fluorescence based instrument intended to be used for th |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ID NOW 88037536 not registered Live/Pending |
Alere Scarborough, Inc. 2018-07-13 |
![]() ID NOW 88037535 not registered Live/Pending |
Alere Scarborough, Inc. 2018-07-13 |
![]() ID NOW 88037533 not registered Live/Pending |
Alere Scarborough, Inc. 2018-07-13 |