SMARTMED

GUDID 00860008514059

M. J. Winston International, Ltd.

Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial

• Primary Device ID: 00860008514059
• NIH Device Record Key: 2d72a2d5-e7dc-4dd1-8156-b6d7fd57aad8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SMARTMED
• Version Model Number: cslarge24
• Company DUNS: 144927378
• Company Name: M. J. Winston International, Ltd.
• 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: 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us
• Phone: 714-582-2715
• Email: info@smartmed.us

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860008514059 [Primary]

FDA Product Code

• NAC: Dressing, Wound, Hydrophilic

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: 2023-08-03
• Device Publish Date: 2023-07-26