INFOV.A.C. ™

GUDID 00878237001738

Infovac Therapy System

KCI USA, INC.

Negative-pressure wound therapy system pump, electric

• Primary Device ID: 00878237001738
• NIH Device Record Key: e8021449-54d6-4d55-9859-0b3936201d8f
• Commercial Distribution Discontinuation: 2021-01-29
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: INFOV.A.C. ™
• Version Model Number: M8259999
• Company DUNS: 102726734
• Company Name: KCI USA, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00878237001738 [Primary]

FDA Product Code

• OMP: Negative Pressure Wound Therapy Powered Suction Pump

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2021-02-01
• Device Publish Date: 2016-09-24

On-Brand Devices [INFOV.A.C. ™]

• 00878237008195: Infovac Therapy System
• 00878237001738: Infovac Therapy System