NOVAPLUS V11440-512

GUDID 50885380057487

Cold Pack, Instant, Non-Sweat

CARDINAL HEALTH 200, LLC

Hot/cold therapy pack, single-use

• Primary Device ID: 50885380057487
• NIH Device Record Key: 5b51992e-e5fa-42e4-bb0a-9722fee46fcb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NOVAPLUS
• Version Model Number: V11440-512
• Catalog Number: V11440-512
• Company DUNS: 112164780
• Company Name: CARDINAL HEALTH 200, LLC
• 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: 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885380057489 [Primary]
GS1	20885380057486 [Package]; Contains: 10885380057489; Package: BOX [12 Units]; In Commercial Distribution
GS1	50885380057487 [Package]; Contains: 20885380057486; Package: CASE [4 Units]; In Commercial Distribution

FDA Product Code

• IMD: PACK, HOT OR COLD, DISPOSABLE

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: 2019-05-20
• Device Publish Date: 2019-05-10

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