V.A.C.VIA™

GUDID 00849554003750

VAC VIA 250ml Canister

KCI USA, INC.

Negative-pressure wound therapy system canister

• Primary Device ID: 00849554003750
• NIH Device Record Key: c37ac78b-964a-4b1e-b27d-2f4126c5964e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V.A.C.VIA™
• Version Model Number: VIACAN05
• 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	00849554002289 [Package]; Package: 5 Pack [5 Units]; In Commercial Distribution
GS1	00849554003750 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132741

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: 4
• Public Version Date: 2018-08-20
• Device Publish Date: 2016-09-05

On-Brand Devices [V.A.C.VIA™ ]

• 00849554003750: VAC VIA 250ml Canister
• 00849554003156: VAC Via System Starter Kit
• 00849554002388: VAC Via System 7-Day Kit