Lumax™ TS Pro

GUDID 60888937013339

Lumax™ TS Pro • EMG Module

Coopersurgical, Inc.

Urodynamic measurement system

• Primary Device ID: 60888937013339
• NIH Device Record Key: 80a7cffa-5966-4b5f-b0ed-c59dfcd56e8f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumax™ TS Pro
• Version Model Number: EMG1
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• 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	60888937013339 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K953734

FDA Product Code

• FEM: Accessories, Photographic, For Endoscope (Exclude Light Sources)

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: 2018-07-06
• Device Publish Date: 2016-09-23

On-Brand Devices [Lumax™ TS Pro]

• 60888937013469: Lumax™ TS Pro Fiberoptic Cystometry System Sales Demo Unit
• 60888937013360: Lumax™ TS Pro Fiberoptic Cystometry System
• 60888937013339: Lumax™ TS Pro • EMG Module
• 00888937013382: Lumax™ TS Pro Advanced Software