VersaPulse P20

GUDID 07290109140544

LUMENIS LTD.

General/multiple surgical solid-state laser system

• Primary Device ID: 07290109140544
• NIH Device Record Key: 2a19b98f-6d20-4617-9a45-10e55d82773f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VersaPulse P20
• Version Model Number: VersaPulse P20
• Company DUNS: 600166524
• Company Name: LUMENIS LTD.
• 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: false
• Lot Batch: false
• Serial Number: true
• 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

Customer Support Contacts

• Phone: 408-764-3000
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109140544 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100228

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2016-08-23

On-Brand Devices [VersaPulse P20]

• 07290109140544: VersaPulse P20
• 07290109146317: VersaPulse P20
• 07290109147154: VERSAPULSE P20