Wittmann Patch

GUDID 00810805000187

For temporary bridging of abdominal wall openings where primary closure is not possible and/or repeat abdominal entries are necessary.

PRESERVATION SOLUTIONS INC

Negative-pressure wound therapy open-abdomen dressing

• Primary Device ID: 00810805000187
• NIH Device Record Key: f9bf4a75-3e97-4cea-b493-2895c8d65b78
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Wittmann Patch
• Version Model Number: EWP2040
• Company DUNS: 090266979
• Company Name: PRESERVATION SOLUTIONS INC
• Device Count: 1
• 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: 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

Customer Support Contacts

• Phone: 2627236715
• Email: brader@preservationsolutions.com
• Phone: 2627236715
• Email: brader@preservationsolutions.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810805000187 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K983753

FDA Product Code

• FTL: Mesh, Surgical, Polymeric

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-10-22

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• 00810805000187 - Wittmann Patch: 2018-07-06For temporary bridging of abdominal wall openings where primary closure is not possible and/or repeat abdominal entries are necessary.
• 00810805000187 - Wittmann Patch: 2018-07-06 For temporary bridging of abdominal wall openings where primary closure is not possible and/or repeat abdominal entries are nece
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