VS3 Bifurcated Light Cable for MMS 560-6318

GUDID 18130400103571

VISIONSENSE LTD.

Fibreoptic light cable Fibreoptic light cable

• Primary Device ID: 18130400103571
• NIH Device Record Key: 138a9d32-e74f-48c5-911d-6a988c1d3f83
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VS3 Bifurcated Light Cable for MMS
• Version Model Number: VS3-MMS
• Catalog Number: 560-6318
• Company DUNS: 532199478
• Company Name: VISIONSENSE LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	18130400103571 [Primary]

FDA Product Code

• FST: Light, Surgical, Fiberoptic

Sterilization

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

[18130400103571]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

[18130400103571]

Hydrogen Peroxide;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

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