Volk Viva

GUDID 00811608014708

VOLK OPTICAL INC.

Ophthalmic fundus camera Ophthalmic fundus camera Ophthalmic fundus camera Ophthalmic fundus camera Ophthalmic fundus camera Ophthalmic fundus camera Ophthalmic fundus camera

• Primary Device ID: 00811608014708
• NIH Device Record Key: ab7f2cc5-6b30-4b23-9c0f-300722a31f11
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Volk Viva
• Version Model Number: VVIVA1A
• Company DUNS: 071125835
• Company Name: VOLK OPTICAL INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 440-942-6161
• Email: peter.chen@volk.com
• Phone: 440-942-6161
• Email: peter.chen@volk.com
• Phone: 440-942-6161
• Email: peter.chen@volk.com
• Phone: 440-942-6161
• Email: peter.chen@volk.com
• Phone: 440-942-6161
• Email: peter.chen@volk.com
• Phone: 440-942-6161
• Email: peter.chen@volk.com
• Phone: 440-942-6161
• Email: peter.chen@volk.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811608014708 [Primary]

FDA Product Code

• PJZ: Camera, Ophthalmic, General-Use

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-15
• Device Publish Date: 2024-04-05

On-Brand Devices [Volk Viva]

• 00811608014739: VVIVA1B
• 00811608014708: VVIVA1A