RespArray NIBP hose

GUDID 06944413824775

Edan Instruments, Inc.

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• Primary Device ID: 06944413824775
• NIH Device Record Key: f6259a04-ffba-42fa-9fee-0d7bf85ed74f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RespArray NIBP hose
• Version Model Number: 01.57.472338
• Company DUNS: 529173163
• Company Name: Edan Instruments, Inc.
• Device Count: 1
• DM Exempt: true
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06944413824775 [Primary]
GS1	16944413824772 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220308

FDA Product Code

• DXQ: Blood Pressure Cuff

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: 2022-09-09
• Device Publish Date: 2022-09-01

On-Brand Devices [RespArray NIBP hose]

• 06944413826205: 01.57.472399
• 06944413824775: 01.57.472338