Finapres

GUDID 08719327003763

Valsalva Assembly

Finapres Medical Systems B.V.

Patient monitoring system module, blood pressure, noninvasive

• Primary Device ID: 08719327003763
• NIH Device Record Key: 201d47b5-c5f2-4ef5-9cc3-bec1d3bdb4f0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Finapres
• Version Model Number: Valsalva Assembly
• Company DUNS: 489470686
• Company Name: Finapres Medical Systems B.V.
• 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	08719327003763 [Primary]

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

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: 2022-06-02
• Device Publish Date: 2022-05-25