VS3 Iridium - Light Integrator (Beamcombiner) 161-0001

GUDID 18130400103625

VISIONSENSE LTD.

Endoscope video camera

• Primary Device ID: 18130400103625
• NIH Device Record Key: e80bbc08-d941-400a-9e38-dc31361c8ce9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VS3 Iridium - Light Integrator (Beamcombiner)
• Version Model Number: VS3-IR
• Catalog Number: 161-0001
• 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	18130400103625 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K152204

FDA Product Code

• GWG: Endoscope, Neurological

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-11-23

On-Brand Devices [VS3 Iridium - Light Integrator (Beamcombiner)]

• 18130400103625: VS3-IR
• 10884521817555: VS3-IR