blue endo

GUDID 14714127863150

Anti fog solution alcohol free

UNIMAX MEDICAL SYSTEMS INC.

Endoscope antifog solution

• Primary Device ID: 14714127863150
• NIH Device Record Key: 42a71003-8d13-4efb-b5eb-fc137435af53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: blue endo
• Version Model Number: 73-000100
• Company DUNS: 658122465
• Company Name: UNIMAX MEDICAL SYSTEMS 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04714127863153 [Primary]
GS1	14714127863150 [Package]; Contains: 04714127863153; Package: Box [20 Units]; In Commercial Distribution
GS1	24714127863157 [Package]; Package: Carton [10 Units]; In Commercial Distribution

FDA Product Code

• OCT: Anti Fog Solution And Accessories, Endoscopy

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-28
• Device Publish Date: 2024-06-20

On-Brand Devices [blue endo]

• 14714127863181: Smoke evacuation tubing
• 14714127863150: Anti fog solution alcohol free