Synvisc

GUDID 03770034301172

UNIVERDERM

Synovial fluid supplementation medium

• Primary Device ID: 03770034301172
• NIH Device Record Key: 35b75d9d-ae03-4c54-bf3e-e4915e1ad1e9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Synvisc
• Version Model Number: One
• 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	03770034301172 [Primary]

FDA Product Code

• MOZ: Acid, Hyaluronic, Intraarticular

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: 2025-03-21
• Device Publish Date: 2025-03-13

On-Brand Devices [Synvisc]

• 03770034301172: One
• 03770034301158: N/A