MiRus Bifurcated Illuminator 012361

GUDID 00810025485344

LUMITEX, INC.

Open surgical site internal light

• Primary Device ID: 00810025485344
• NIH Device Record Key: c0399422-4537-4013-a09b-bbea3add8fe2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MiRus Bifurcated Illuminator
• Version Model Number: 17-518
• Catalog Number: 012361
• Company DUNS: 108631797
• Company Name: LUMITEX, 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: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810025485344 [Primary]

FDA Product Code

• FDG: Retractor, Fiberoptic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-21
• Device Publish Date: 2023-08-11

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• 00812432022396 - Spineart Wolf Cable Adaptor: 2023-08-21
• 00812432022921 - Spineart Olympus Cable Adaptor: 2023-08-21
• 00810025485344 - MiRus Bifurcated Illuminator: 2023-08-21
• 00810025485344 - MiRus Bifurcated Illuminator: 2023-08-21
• 00812432021559 - Spineart Storz Cable Adaptor: 2023-08-21