FilmArray® 2.0 Instrument

GUDID 00815381029058

Refurbished IVD Instrument (FilmArray® 2.0 Instrument).

BIOFIRE DIAGNOSTICS, LLC

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• Primary Device ID: 00815381029058
• NIH Device Record Key: c8cf9204-89bf-4f12-b656-7582ab2b5aa8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FilmArray® 2.0 Instrument
• Version Model Number: FLM2-ASY-0001-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 Identifiers

Device Issuing Agency	Device ID
GS1	00815381029058 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143178

FDA Product Code

• NSU: Instrumentation For Clinical Multiplex Test Systems

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: 2021-06-29
• Device Publish Date: 2021-06-21

On-Brand Devices [FilmArray® 2.0 Instrument]

• 00815381020048: Refurbished IVD Instrument (FilmArray® 2.0 Instrument).
• 00815381020031: IVD Instrument (FilmArray® 2.0 Instrument).
• 00815381029058: Refurbished IVD Instrument (FilmArray® 2.0 Instrument).