Uphold™ LITE

GUDID 08714729839200

Vaginal Support System

BOSTON SCIENTIFIC CORPORATION

Pelvic organ prolapse surgical mesh, synthetic polymer

• Primary Device ID: 08714729839200
• NIH Device Record Key: ba7e6476-00df-446f-8f3f-61271d151a65
• Commercial Distribution Discontinuation: 2019-07-23
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Uphold™ LITE
• Version Model Number: M0068318170
• 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	08714729839200 [Primary]

FDA Product Code

• OTP: Mesh, surgical, synthetic, urogynecologic, for pelvic organ prolapse, transvaginally placed

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-12-13
• Device Publish Date: 2015-09-24

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