Cardinal Health

GUDID 30817357020190

Cardinal Health Flexiport Adult

HYGIA HEALTH SERVICES, INC.

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• Primary Device ID: 30817357020190
• NIH Device Record Key: 181d81fa-c900-48cf-8d89-bd31d1ea8b4c
• Commercial Distribution Discontinuation: 2019-07-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Cardinal Health
• Version Model Number: 30503-13
• Company DUNS: 177939027
• Company Name: HYGIA HEALTH SERVICES, 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	10817357020196 [Primary]
GS1	30817357020190 [Package]; Contains: 10817357020196; Package: Box [20 Units]; Discontinued: 2021-03-19; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K032821

FDA Product Code

• NPP: Reprocessed Blood Pressure Cuff

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-03-19
• Device Publish Date: 2016-09-28

On-Brand Devices [Cardinal Health]

• 30817357022217: Cardinal Health Flexiport Large Adult
• 30817357022200: Cardinal Health Flexiport Small Adult
• 30817357021623: Cardinal Health Flexiport One-Tube Bayonet, Adult
• 30817357020473: Cardinal Health Flexiport Adult Long
• 30817357020190: Cardinal Health Flexiport Adult