BIOFIRE® FILMARRAY® Tropical Fever Panel

GUDID 00815381021007

IVD reagent kit containing 6 tests.

BIOFIRE DIAGNOSTICS, LLC

Multiple-type tropical pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)

• Primary Device ID: 00815381021007
• NIH Device Record Key: a1248d34-618b-40e1-9ae9-4e7d6320e92b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BIOFIRE® FILMARRAY® Tropical Fever Panel
• Version Model Number: 424803
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00815381021007 [Primary]

FDA Product Code

• QMV: Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-02-26
• Device Publish Date: 2025-02-18

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