3M™ V.A.C. Veraflo Cleanse™ ULTVCL05MD

GUDID 00849554014763

3M™ V.A.C. Veraflo Cleanse™ Dressing, ULTVCL05MD, Medium, Cavilon Warning Label, 5/CS

KCI USA, INC.

Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing Irrigation negative-pressure wound therapy dressing

• Primary Device ID: 00849554014763
• NIH Device Record Key: 6f8dcd63-5e69-4435-834f-e8de5035f91b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3M™ V.A.C. Veraflo Cleanse™
• Version Model Number: ULTVCL05MD
• Catalog Number: ULTVCL05MD
• Company DUNS: 102726734
• Company Name: KCI USA, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00849554014022 [Primary]
GS1	00849554014763 [Package]; Contains: 00849554014022; 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: 2024-04-26
• Device Publish Date: 2024-04-18

Devices Manufactured by KCI USA, INC.

• 00849554014763 - 3M™ V.A.C. Veraflo Cleanse™: 2024-04-263M™ V.A.C. Veraflo Cleanse™ Dressing, ULTVCL05MD, Medium, Cavilon Warning Label, 5/CS
• 00849554014763 - 3M™ V.A.C. Veraflo Cleanse™: 2024-04-26 3M™ V.A.C. Veraflo Cleanse™ Dressing, ULTVCL05MD, Medium, Cavilon Warning Label, 5/CS
• 00849554014770 - 3M™ V.A.C. Veraflo™: 2024-04-26 3M™ V.A.C. Veraflo™ Dressing, ULTVFL05SM, Small, Cavilon Warning Label, 5/CS
• 00849554014787 - 3M™ V.A.C. Veraflo™: 2024-04-26 3M™ V.A.C. Veraflo™ Dressing, ULTVFL05MD, Medium, Cavilon Warning Label, 5/CS
• 00849554014794 - 3M™ V.A.C. Veraflo™: 2024-04-26 3M™ V.A.C. Veraflo™ Dressing, ULTVFL05LG, Large, Cavilon Warning Label, 5/CS
• 50849554013860 - 3M™ V.A.C.®: 2024-03-13 3M™ V.A.C.® Peel and Place Dressing Kit, EZ5SML, Small, 5/CS
• 50849554015000 - 3M™ V.A.C.®: 2024-03-13 3M™ V.A.C.® Peel and Place Dressing Kit, EZ5MED, Medium, 5/CS
• 50849554013884 - 3M™ V.A.C.®: 2024-03-13 3M™ V.A.C.® Peel and Place Dressing Kit, EZ5LRG, Large, 5/CS
• 50849554014027 - 3M™ Veraflo™: 2023-07-20 3M™ V.A.C. Veraflo Cleanse™ Dressing, ULTVCL05MD, Medium, Cavilon Warning Label, 5/CS