SENSAT.R.A.C.™

GUDID 00849554002531

Sensatrac Pad

KCI USA, INC.

Negative-pressure wound therapy tubing set

• Primary Device ID: 00849554002531
• NIH Device Record Key: 0918fd52-0ef8-4163-8dfb-d8e58108e6f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SENSAT.R.A.C.™
• Version Model Number: M8275057/10
• 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	00849554002531 [Primary]
GS1	00849554002586 [Package]; 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: 2018-08-02
• Device Publish Date: 2016-09-05

On-Brand Devices [SENSAT.R.A.C.™ ]

• 00878237001141: Sensatrac Pad
• 00849554002531: Sensatrac Pad