LightTrail™ Single Use

GUDID 08714729939771

Laser Fiber

BOSTON SCIENTIFIC CORPORATION

General/multiple surgical laser system beam guide, single-use

• Primary Device ID: 08714729939771
• NIH Device Record Key: 3dad3892-61ac-4b03-9e3b-59cf0fbb0aa3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LightTrail™ Single Use
• Version Model Number: M0068F64520
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729939771 [Primary]

FDA Product Code

• GEX: Powered laser surgical instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-04-07
• Device Publish Date: 2018-06-15

On-Brand Devices [LightTrail™ Single Use]

• 08714729939801: Laser Fiber
• 08714729939795: Laser Fiber
• 08714729939788: Laser Fiber
• 08714729939771: Laser Fiber
• 08714729939764: Laser Fiber