Juvederm

GUDID 03770034301011

UNIVERDERM

Dermal tissue reconstructive material, microbe-derived, anaesthetic

• Primary Device ID: 03770034301011
• NIH Device Record Key: 577df2b8-580e-4d08-af2b-83441f587d1c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Juvederm
• Version Model Number: Voluma
• Company DUNS: 281488639
• Company Name: UNIVERDERM
• 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	03770034301011 [Primary]
GS1	03770034301073 [Package]; Package: [2 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P110033

FDA Product Code

• LMH: Implant, Dermal, For Aesthetic Use

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-05
• Device Publish Date: 2024-02-26

On-Brand Devices [Juvederm]

• 03770034301011: Voluma
• 03770034301004: Volbella