SafeMask

GUDID 00686864060871

Artisan E/L white L3

AMD Medicom Inc

Surgical/medical face mask, non-antimicrobial, single-use

• Primary Device ID: 00686864060871
• NIH Device Record Key: 28899956-3cab-4afd-8368-1da5124b184e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SafeMask
• Version Model Number: 221414
• Company DUNS: 256880576
• Company Name: AMD Medicom Inc
• Device Count: 50
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1 514-636-6262
• Email: mkansou@medicom.ca
• Phone: +1 514-636-6262
• Email: mkansou@medicom.ca
• Phone: +1 514-636-6262
• Email: mkansou@medicom.ca
• Phone: +1 514-636-6262
• Email: mkansou@medicom.ca
• Phone: +1 514-636-6262
• Email: mkansou@medicom.ca
• Phone: +1 514-636-6262
• Email: mkansou@medicom.ca
• Phone: +1 514-636-6262
• Email: mkansou@medicom.ca
• Phone: +1 514-636-6262
• Email: mkansou@medicom.ca
• Phone: +1 514-636-6262
• Email: mkansou@medicom.ca

Device Identifiers

Device Issuing Agency	Device ID
GS1	00686864060871 [Unit of Use]
GS1	10686864060878 [Primary]

FDA Product Code

• FXX: Mask, Surgical

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: 2024-11-20
• Device Publish Date: 2024-11-12

On-Brand Devices [SafeMask]

• 00686864060888: Vision E/L white L3
• 00686864060871: Artisan E/L white L3
• 00686864060864: Artisan E/L black L3
• 00686864060857: Artisan E/L blue L3
• 00686864060840: Artisan E/L blue L2