V.A.C.®

GUDID 00878237001646

V.A.C. DRAPE

KCI USA, INC.

Negative-pressure wound therapy system drape

• Primary Device ID: 00878237001646
• NIH Device Record Key: 4238e3aa-f8e5-4a54-bdc6-ae7b3868d6b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V.A.C.®
• Version Model Number: M6275009/10
• 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: 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	00878237001479 [Package]; Package: 10 Pack [10 Units]; In Commercial Distribution
GS1	00878237001646 [Primary]

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