DEJA VU 28000-02Y

GUDID 10885380180187

Maxi Yellow Vessel Loops, Bulk Non-Sterile, 1000EA/CS

Cardinal Health 200, LLC

Surgical vessel loop

• Primary Device ID: 10885380180187
• NIH Device Record Key: af86a3ea-cef5-429f-92af-019a207884ce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DEJA VU
• Version Model Number: 28000-02Y
• Catalog Number: 28000-02Y
• Company DUNS: 961027315
• Company Name: Cardinal Health 200, LLC
• Device Count: 1000
• DM Exempt: true
• 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: false
• Expiration Date: false
• 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	10885380180187 [Unit of Use]
GS1	50885380180185 [Primary]

FDA Product Code

• KDC: INSTRUMENT, SURGICAL, DISPOSABLE

Sterilization

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

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

[10885380180187]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-05-04
• Device Publish Date: 2021-04-26

On-Brand Devices [DEJA VU]

• 10885380180187: Maxi Yellow Vessel Loops, Bulk Non-Sterile, 1000EA/CS
• 50885380179660: Cardinal Health Vessel Loops Maxi White