BioFire® Respiratory Panel 2.1 EUA

GUDID 00815381020482

IVD reagent kit containing 30 tests.

BIOFIRE DIAGNOSTICS, LLC

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• Primary Device ID: 00815381020482
• NIH Device Record Key: acd685b4-c0b1-458b-b267-4be17b47f0f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BioFire® Respiratory Panel 2.1 EUA
• Version Model Number: 423738
• Company DUNS: 079280262
• Company Name: BIOFIRE DIAGNOSTICS, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	00815381020482 [Primary]

FDA Product Code

• QJR: Reagents, 2019-Novel Coronavirus Nucleic Acid

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: 2020-12-03
• Device Publish Date: 2020-11-25

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