FilmArray® Pneumonia Panel plus (Pneumoplus)

GUDID 00815381020321

IVD reagent kit containing 6 tests

BIOFIRE DIAGNOSTICS, LLC

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• Primary Device ID: 00815381020321
• NIH Device Record Key: dd3c3681-6afc-430d-8bf8-28341171817b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FilmArray® Pneumonia Panel plus (Pneumoplus)
• Version Model Number: RFIT-ASY-0142
• 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	00815381020321 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181324

FDA Product Code

• QDS: Mers-Cov And Common Respiratory Pathogens Semi-Quantitative And Quantitative Multiplex Nucleic Acid Detection System

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: 2019-01-14
• Device Publish Date: 2018-12-12

On-Brand Devices [FilmArray® Pneumonia Panel plus (Pneumoplus)]

• 00815381020321: IVD reagent kit containing 6 tests
• 00815381020314: IVD reagent kit containing 30 tests