Nodify Lung (PR) 56

GUDID G292560

Sample Collection Kit

Biodesix, Inc.

Blood collection set, invasive

• Primary Device ID: G292560
• NIH Device Record Key: 2a0e1114-67a1-4279-92b5-d418fe305684
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nodify Lung (PR)
• Version Model Number: 2
• Catalog Number: 56
• Company DUNS: 809047215
• Company Name: Biodesix, Inc.
• 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: true
• Expiration Date: true
• 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
HIBCC	G292560 [Primary]

FDA Product Code

• PQD: Blood Specimen Collection Convenience Kit (Excludes Hiv)

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: 2023-03-16
• Device Publish Date: 2023-03-08

Devices Manufactured by Biodesix, Inc.

• G29259080 - Capillary Blood Specimen Collection Supplemental Pack: 2026-02-18 Capillary blood specimen collection pack
• G29251120 - Nodify: 2026-02-18 Specimen Collection Kit
• G29252150 - IQLung: 2026-02-18 Specimen Collection Kit
• G29255100 - IQLung (PR): 2026-02-18 Specimen Collection Kit
• G29256090 - Nodify (PR): 2026-02-18 Specimen Collection Kit
• G29252140 - IQLung: 2026-02-11 Specimen Collection Kit
• G29255090 - IQLung (PR): 2026-02-11 Specimen Collection Kit
• G29256080 - Nodify (PR): 2026-02-04 Sample Collection Kit