HARTMANN

GUDID 26942327010172

Winner Medical Co., Ltd.

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

• Primary Device ID: 26942327010172
• NIH Device Record Key: f99e8ce7-4ea6-4e50-a296-6a6822e20598
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HARTMANN
• Version Model Number: 603-017204
• Company DUNS: 530629351
• Company Name: Winner Medical Co., 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	16942327010175 [Primary]
GS1	26942327010172 [Package]; Contains: 16942327010175; Package: [10 Units]; Discontinued: 2025-08-28; Not in Commercial Distribution
GS1	36942327010179 [Package]; Package: [24 Units]; Discontinued: 2025-08-28; Not in Commercial Distribution

FDA Product Code

• NAD: Dressing, Wound, Occlusive

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: 2025-09-05
• Device Publish Date: 2025-08-28

On-Brand Devices [HARTMANN]

• 16942327072449: 603-017184
• 26942327071951: 603-017196
• 26942327056330: 603-017212
• 26942327025497: 603-017190
• 26942327010172: 603-017204