DERMATAC™ FILM

GUDID 00849554007970

DERMATAC™ FILM

KCI USA, INC.

Synthetic polymer semi-permeable film dressing, adhesive, sterile

• Primary Device ID: 00849554007970
• NIH Device Record Key: fc9d126b-a6a3-4226-823a-bcab1ad9571c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DERMATAC™ FILM
• Version Model Number: DTAC10FLM
• Company DUNS: 102726734
• Company Name: KCI USA, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00849554007963 [Primary]
GS1	00849554007970 [Package]; Contains: 00849554007963; Package: 10 Pack [10 Units]; 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: 2019-12-18
• Device Publish Date: 2019-12-10

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