| Primary Device ID | 00815381020307 |
| NIH Device Record Key | 05d11f73-ac00-4478-8773-6259c7b76bb3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FilmArray® Respiratory Panel 2 plus (RP2plus) |
| Version Model Number | RFIT-ASY-0137 |
| Catalog Number | RFIT-ASY-0137 |
| Company DUNS | 079280262 |
| Company Name | BIOFIRE DIAGNOSTICS, LLC |
| 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 | true |
| 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 | 00815381020307 [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 | 2018-07-06 |
| Device Publish Date | 2017-12-22 |
| 00815381020307 | IVD reagent kit containing 6 tests |
| 00815381020291 | IVD reagent kit containing 30 tests |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FILMARRAY 85939258 4554601 Live/Registered |
BioFire Diagnostics, Inc. 2013-05-22 |
![]() FILMARRAY 77083897 3761522 Live/Registered |
BIOFIRE DIAGNOSTICS, LLC 2007-01-16 |