| 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 |