V.A.C.VIA™ GRANUFOAM™

GUDID 00849554003767

VAC VIA Dressing Medium Featuring a Granufoam Spiral Dressing

KCI USA, INC.

Negative-pressure wound therapy system foam dressing Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial

• Primary Device ID: 00849554003767
• NIH Device Record Key: 90b80aab-6e4f-4c64-ab6a-b4c401b1e640
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V.A.C.VIA™ GRANUFOAM™
• Version Model Number: VIAGFM05
• 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	00849554002296 [Package]; Package: 5 Pack [5 Units]; In Commercial Distribution
GS1	00849554003767 [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: 2018-07-06
• Device Publish Date: 2016-09-05

On-Brand Devices [V.A.C.VIA™ GRANUFOAM™]

• 00849554003774: Vac Via Dressing Small
• 00849554003767: VAC VIA Dressing Medium Featuring a Granufoam Spiral Dressing