MAGENTIQ-COLO (ME-APDS)

GUDID 07290020140012

MAGENTIQ EYE LTD

Endoscopic video image interpretive unit

• Primary Device ID: 07290020140012
• NIH Device Record Key: a1549dc8-e81d-4dca-b908-574b939db8f0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAGENTIQ-COLO (ME-APDS)
• Version Model Number: APDS-DA-CU
• Company DUNS: 600326787
• Company Name: MAGENTIQ EYE LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com
• Phone: +972772018838
• Email: info@magentiq.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290020140012 [Primary]

FDA Product Code

• QNP: Gastrointesinal Lesion Software Detection System

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: 2025-08-29
• Device Publish Date: 2025-08-21