LithoVue M0067913600

GUDID 08714729874812

Single-Use Digital Flexible Ureteroscope

BOSTON SCIENTIFIC CORPORATION

Flexible video ureteroscope, single-use

• Primary Device ID: 08714729874812
• NIH Device Record Key: 898d81bd-38a9-4d2e-8ddb-0b2aa688864d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LithoVue
• Version Model Number: M0067913600
• Catalog Number: M0067913600
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	08714729874812 [Primary]

FDA Product Code

• FGB: Ureteroscope and accessories, flexible/rigid

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2025-07-08
• Device Publish Date: 2016-09-24

On-Brand Devices [LithoVue]

• 08714729891932: Touch PC
• 08714729891901: Touch PC
• 08714729974789: Touch PC
• 08714729974819: Touch PC
• 08714729874522: System Workstation
• 08714729974826: Touch PC
• 08714729974802: Touch PC
• 08714729974796: Touch PC
• 08714729880929: System Workstation
• 08714729880912: System Workstation
• 08714729891840: System Workstation
• 08714729874812: Single-Use Digital Flexible Ureteroscope
• 08714729874805: Single-Use Digital Flexible Ureteroscope