WoundPro+ Collection Canister

GUDID 00851978007665

WoundPro+ 300cc Basic Collection Canister with 8 foot tubing, Case of 16

Pensar Medical, LLC

Negative-pressure wound therapy system canister

• Primary Device ID: 00851978007665
• NIH Device Record Key: 2acb0934-244a-4410-8325-8ab0bd88ab6a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WoundPro+ Collection Canister
• Version Model Number: 8463540 0941
• Company DUNS: 079262228
• Company Name: Pensar Medical, LLC
• Device Count: 16
• 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: 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	00851978007665 [Unit of Use]
GS1	10851978007662 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150960

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-26
• Device Publish Date: 2025-03-18

On-Brand Devices [WoundPro+ Collection Canister]

• 00851978007627: WoundPro+ 300cc Basic Collection Canister with 5 foot tubing, Case of 16
• 00851978007665: WoundPro+ 300cc Basic Collection Canister with 8 foot tubing, Case of 16