CoolTouch

GUDID 00859932006143

Fiber Optic Catheter

NEW STAR LASERS, INC.

General/multiple surgical solid-state laser system

• Primary Device ID: 00859932006143
• NIH Device Record Key: 5d4f77b0-da13-4980-9770-88f13a233f21
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CoolTouch
• Version Model Number: 7420-0018
• Company DUNS: 877266163
• Company Name: NEW STAR LASERS, 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: true
• 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	00859932006143 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-20

On-Brand Devices [CoolTouch]

• 00859932006327: Pullback Device
• 00859932006310: Pullback Device
• 10859932006300: Cryogen Cooling
• 10859932006294: Cryogen Cooling
• 00859932006266: Pullback Device
• 00859932006259: Pullback Device
• 00859932006181: Fiber Optic Catheter
• 00859932006150: Fiber Optic Catheter
• 00859932006143: Fiber Optic Catheter
• 00859932006136: Fiber Optic Catheter
• 00859932006129: Fiber Optic Catheter
• 00859932006112: Fiber Optic Catheter
• 00859932006105: Fiber Optic Catheter
• 00859932006099: Fiber Optic Catheter
• 00859932006082: Fiber Optic Catheter