Primary Device ID | 00815381020376 |
NIH Device Record Key | 669a1a0e-6f36-472f-b593-a4442708f070 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BIOFIRE ® SPOTFIRE ® Module |
Version Model Number | FAST-ASY-0002-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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815381020376 [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 | 2023-04-14 |
Device Publish Date | 2023-04-06 |
00815381020376 | Used IVD Instrument (SPOTFIRE® Module). |
00815381020369 | IVD Instrument (SPOTFIRE ® Module). |
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 |