DUOVISC

GUDID 00380651831353

DUOVISC (0.40PRO/0.35VIS)

Alcon Laboratories, Inc.

Aqueous/vitreous humour replacement medium kit

• Primary Device ID: 00380651831353
• NIH Device Record Key: 51b767dc-46b6-4b46-a0ca-b28731b69882
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DUOVISC
• Version Model Number: 8065183135
• Company DUNS: 008018525
• Company Name: Alcon Laboratories, Inc.
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380651831353 [Primary]

FDA Product Code

• LZP: Aid, Surgical, Viscoelastic

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: 2018-03-29
• Device Publish Date: 2015-03-31

On-Brand Devices [DUOVISC]

• 00380651999077: DuoVisc Viscoelastic System
• 00380651831506: DUOVISC (0.55PRO/0.50VIS)
• 00380651831353: DUOVISC (0.40PRO/0.35VIS)