Rapid SLT

GUDID 00811608019802

VOLK OPTICAL INC.

Gonioscope

• Primary Device ID: 00811608019802
• NIH Device Record Key: c75e40ef-b2c1-487d-b87d-368568f8100c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rapid SLT
• Version Model Number: VLUMSLT
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811608019802 [Primary]

FDA Product Code

• HKS: Prism, Gonioscopic

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: 2025-08-15
• Device Publish Date: 2025-08-07

On-Brand Devices [Rapid SLT]

• 00811608019581: VMSLT
• 00811608019802: VLUMSLT