V.A.C.ULTA™

GUDID 00849554006775

Solution Container Hanger Arm Extension

KCI USA, INC.

Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder Frame/rail/pole device holder

• Primary Device ID: 00849554006775
• NIH Device Record Key: de979d07-8dcf-463e-a4a9-c2ef67b5b01d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V.A.C.ULTA™
• Version Model Number: ULTEXT0500
• Company DUNS: 102726734
• Company Name: KCI USA, INC.
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	00849554006775 [Primary]
GS1	00849554006782 [Package]; Package: 5 Pack [5 Units]; In Commercial Distribution

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: 3
• Public Version Date: 2019-06-07
• Device Publish Date: 2018-04-03

On-Brand Devices [V.A.C.ULTA™]

• 00849554006775: Solution Container Hanger Arm Extension
• 00849554001244: VAC ULTA THERAPY SYSTEM
• 00849554000636: VAC ULTA THERAPY SYSTEM