| Primary Device ID | 00815381020727 |
| NIH Device Record Key | 436893db-15ac-46bd-b5b5-151908891765 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIOFIRE® SPOTFIRE® Respiratory/Sore Throat (R/ST) Panel Mini |
| Version Model Number | 424537 |
| 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 | 00815381020727 [Primary] |
| NSU | Instrumentation For Clinical Multiplex Test Systems |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-08-05 |
| Device Publish Date | 2024-07-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BIOFIRE 97123037 not registered Live/Pending |
Biofire Technologies Inc. 2021-11-12 |
![]() BIOFIRE 88852597 not registered Live/Pending |
Biofire Technologies Inc. 2020-03-30 |
![]() BIOFIRE 87204256 not registered Live/Pending |
Biofire Technologies Inc. 2016-10-14 |
![]() BIOFIRE 85981790 4534857 Live/Registered |
Idaho Technology, Inc. 2012-08-09 |
![]() BIOFIRE 79057952 3722496 Live/Registered |
CONCEPT Gesellschaft für kreative; Produktentwicklung Gesellschaft m.b.H. 2008-07-11 |