V.A.C.®

GUDID 00878237001295

VAC TUBING CAP

KCI USA, INC.

Negative-pressure wound therapy tubing set

• Primary Device ID: 00878237001295
• NIH Device Record Key: 9f8d4fa4-7ce1-404b-8727-3c45c3f81237
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V.A.C.®
• Version Model Number: M6275069/5 M6275069/10
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00878237001257 [Primary]
GS1	00878237001295 [Package]; Contains: 00878237001257; Package: 10 Pack [10 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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-08-17
• Device Publish Date: 2017-11-22

On-Brand Devices [V.A.C.® ]

• 00878237001646: V.A.C. DRAPE
• 00878237001325: Vac Abdominal Dressing Featuring Sensatrac Technology
• 00878237001295: VAC TUBING CAP
• 00878237001264: VAC Y-CONNECTOR
• 00849554003385: VAC TUBING CAP
• 00849554003378: VAC Y-CONNECTOR
• 00849554003323: V.A.C. DRAPE
• 00849554003286: VAC Whitefoam dressing Small Foam Only
• 00849554002562: Vac Abdominal Dressing Featuring Sensatrac Technology
• 00849554001336: KCI NPWT Gauze Dressing Large Featuring Sensatrac Technology