3M™ Veraflo™ ULTVCC05MD

GUDID 50849554014065

3M™ V.A.C. Veraflo Cleanse Choice™ Dressing, ULTVCC05MD, Medium, Cavilon Warning Label, 5/CS

KCI USA, INC.

Irrigation negative-pressure wound therapy dressing

• Primary Device ID: 50849554014065
• NIH Device Record Key: ce8a9cdb-86a2-4c3a-a94d-5d673c324f9e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3M™ Veraflo™
• Version Model Number: ULTVCC05MD
• Catalog Number: ULTVCC05MD
• Company DUNS: 102726734
• Company Name: KCI USA, 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: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10849554014067 [Primary]
GS1	50849554014065 [Package]; Contains: 10849554014067; Package: BOX [5 Units]; In Commercial Distribution

FDA Product Code

• OMP: negative pressure wound therapy Powered suction pump

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: 2023-07-20
• Device Publish Date: 2023-07-12

On-Brand Devices [3M™ Veraflo™]

• 50849554014072: 3M™ V.A.C. Veraflo Cleanse Choice™ Dressing, ULTVCC05LG, Large, Cavilon Warning Label, 5/CS
• 50849554014065: 3M™ V.A.C. Veraflo Cleanse Choice™ Dressing, ULTVCC05MD, Medium, Cavilon Warning Label, 5/CS
• 50849554014058: 3M™ V.A.C. Veraflo™ Dressing, ULTVFL05LG, Large, Cavilon Warning Label, 5/CS
• 50849554014041: 3M™ V.A.C. Veraflo™ Dressing, ULTVFL05MD, Medium, Cavilon Warning Label, 5/CS
• 50849554014034: 3M™ V.A.C. Veraflo™ Dressing, ULTVFL05SM, Small, Cavilon Warning Label, 5/CS
• 50849554014027: 3M™ V.A.C. Veraflo Cleanse™ Dressing, ULTVCL05MD, Medium, Cavilon Warning Label, 5/CS