Twilight TWL-0001

GUDID 00860014752704

EVOQ TECHNOLOGIES CORP.

Adaptometer

• Primary Device ID: 00860014752704
• NIH Device Record Key: 7dc1181e-fafb-48a5-9a59-38cc7718eb80
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Twilight
• Version Model Number: V0001P
• Catalog Number: TWL-0001
• Company DUNS: 145199610
• Company Name: EVOQ TECHNOLOGIES CORP.
• 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: 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: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com
• Phone: 8165295712
• Email: info@goevoq.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860014752704 [Primary]

FDA Product Code

• OUM: Adaptometer (Biophotometer), Software-Based Data Acquisition And Stimulus Generation

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: 2026-01-07
• Device Publish Date: 2025-12-30