blue endo

GUDID 14714127863150

Anti fog solution alcohol free

UNIMAX MEDICAL SYSTEMS INC.

Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution Endoscope antifog solution 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