Navigator

GUDID 01816835023911

Navigator, Dual Arm Fixed Pendent

Medical Illumination International Inc.

General utility supply system, ceiling-mounted

• Primary Device ID: 01816835023911
• NIH Device Record Key: d2c2bf2c-8863-4f87-b24a-da26ebe8a206
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Navigator
• Version Model Number: NAV-DAF-
• 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: true
• 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	00816835023912 [Primary]
GS1	01816835023911 [Package]; Contains: 00816835023912; 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