ID NOW RSV

GUDID 10811877010521

A rapid, automated, molecular test for the qualitative detection of respiratory syncytial virus (RSV) nucleic acid in nasopharyngeal specimens.

Alere Scarborough, Inc.

Respiratory syncytial virus (RSV) nucleic acid IVD, kit, nucleic acid technique (NAT)

• Primary Device ID: 10811877010521
• NIH Device Record Key: d3243c46-69da-4d31-8f09-3b282512421f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ID NOW RSV
• Version Model Number: 435-000
• Company DUNS: 154148498
• Company Name: Alere Scarborough, 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: 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	10811877010521 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161375

FDA Product Code

• OCC: Respiratory Virus Panel Nucleic Acid Assay System

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-09-12
• Device Publish Date: 2018-10-29

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