Zetuvit Plus 413739

GUDID 04052199708959

413739 Zetuvit Plus 20 x 60 cm P10

PAUL HARTMANN AG

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

• Primary Device ID: 04052199708959
• NIH Device Record Key: 8417e3fb-8a14-4dd7-a5bf-391d124acbf9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zetuvit Plus
• Version Model Number: 413739 Zetuvit Plus 20 x 60 cm P10
• Catalog Number: 413739
• Company DUNS: 315768788
• Company Name: PAUL HARTMANN AG
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	04052199708942 [Primary]
GS1	04052199708959 [Package]; Contains: 04052199708942; Package: FBX [10 Units]; In Commercial Distribution
GS1	04052199740058 [Package]; Package: CS [2 Units]; In Commercial Distribution

FDA Product Code

• NAC: Dressing, Wound, Hydrophilic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2026-01-21
• Device Publish Date: 2024-12-10

On-Brand Devices [Zetuvit Plus]

• 04052199708959: 413739 Zetuvit Plus 20 x 60 cm P10
• 04052199708935: 413729 Zetuvit Plus 6 x 6 cm P10