Navigator

GUDID 01816835023942

Navigator, Navi-Port Pendent

Medical Illumination International Inc.

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• Primary Device ID: 01816835023942
• NIH Device Record Key: d3472c32-461c-4761-8a76-b747d980ae4f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Navigator
• Version Model Number: NAV-NP-
• Company DUNS: 093357739
• Company Name: Medical Illumination International Inc.
• 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: false
• Lot Batch: false
• Serial Number: true
• 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	00816835023943 [Primary]
GS1	01816835023942 [Package]; Contains: 00816835023943; Package: BOX [1 Units]; In Commercial Distribution

FDA Product Code

• FQO: Table, Operating-Room, Ac-Powered

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: 2023-07-11
• Device Publish Date: 2023-07-03

On-Brand Devices [Navigator]

• 01816835023942: Navigator, Navi-Port Pendent
• 01816835023935: Navigator, Dual Arm Retractable Pendent
• 01816835023928: Navigator, Single Arm Retractable Pendent
• 01816835023911: Navigator, Dual Arm Fixed Pendent
• 01816835023904: Navigator, Single Arm Fixed Pendent