VolparaDoseSR

GUDID 09421904268272

VolparaDoseSR 3.4.2

VOLPARA HEALTH TECHNOLOGIES LIMITED

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• Primary Device ID: 09421904268272
• NIH Device Record Key: 6ec2d45f-b660-4c0e-85df-76b35a342584
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VolparaDoseSR
• Version Model Number: 3.4.2
• Company DUNS: 590762212
• Company Name: VOLPARA HEALTH TECHNOLOGIES LIMITED
• 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• 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	09421904268272 [Primary]

FDA Product Code

• LHO: Instrument, Quality-Assurance, Radiologic

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: 2020-10-02
• Device Publish Date: 2020-09-24

On-Brand Devices [VolparaDoseSR]

• 09421904268043: VolparaDoseSR 3.2
• 09421904268302: VolparaDoseSR 4.0
• 09421904268272: VolparaDoseSR 3.4.2