CoolLipoTM M210273S

GUDID 04059497000273

LEONI Fiber Optics GmbH

General/multiple surgical diode laser system

• Primary Device ID: 04059497000273
• NIH Device Record Key: 143c4d48-e2a5-4956-b301-3d5567f3ad83
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CoolLipoTM
• Version Model Number: CL 320 S
• Catalog Number: M210273S
• Company DUNS: 342703174
• Company Name: LEONI Fiber Optics GmbH
• 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	04059497000037 [Primary]
GS1	04059497000273 [Package]; Contains: 04059497000037; Package: [5 Units]; In Commercial Distribution
GS1	04059497000518 [Package]; Package: [2 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050738

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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-29

On-Brand Devices [CoolLipoTM]

• 04059497000747: CL 500 S
• 04059497000358: CL 320 R
• 04059497000587: CL 500 R
• 04059497000273: CL 320 S