Lumax TS Pro

GUDID 20888937011160

Fiberoptic Pressure Transducer Catheter: Abdominal, 10 French

Coopersurgical, Inc.

Urodynamic catheter

• Primary Device ID: 20888937011160
• NIH Device Record Key: 1036d5cd-3289-495b-bb13-b62c049a1ed7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumax TS Pro
• Version Model Number: 10307-009
• Company DUNS: 801895244
• Company Name: Coopersurgical, Inc.
• Device Count: 1
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888937011166 [Primary]
GS1	20888937011160 [Package]; Contains: 00888937011166; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K953734

FDA Product Code

• FEN: Device, Cystometric, Hydraulic

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: 2018-07-06
• Device Publish Date: 2016-05-09

On-Brand Devices [Lumax TS Pro]

• 00888937014044: Lumax TS Pro Fiberoptic Transmission Cable Reusable • Length: 44" (112 cm)
• 20888937011177: Fiberoptic Pressure Transducer Catheter: Bladder, 10 French
• 20888937011160: Fiberoptic Pressure Transducer Catheter: Abdominal, 10 French
• 20888937011153: Fiberoptic Pressure Transducer Catheter: Bladder, 7 French