Primary Device ID | 00815381029089 |
NIH Device Record Key | 50440d76-c93d-4c6c-9b25-aaef1da4c7ad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FilmArray® Torch Module |
Version Model Number | HTFA-ASY-0003-W |
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 | false |
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 | 00815381029089 [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 | 2021-06-29 |
Device Publish Date | 2021-06-21 |
00815381020284 | Refurbished IVD instrument (Torch Module) |
00815381020277 | IVD Instrument (FilmArray® Torch Module). |
00815381029089 | Refurbished IVD Instrument (FilmArray® Torch Module) |
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 |