VersaCut™

GUDID 07290109143095

LUMENIS LTD.

Tissue morcellation system

• Primary Device ID: 07290109143095
• NIH Device Record Key: 54b3001c-f63e-48b7-8f6b-614617f658b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VersaCut™
• Version Model Number: Steralization Tray
• 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: false
• 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	07290109143095 [Primary]

FDA Product Code

• GCJ: Laparoscope, General & Plastic Surgery

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-11-26
• Device Publish Date: 2016-10-10

On-Brand Devices [VersaCut™]

• 07290109143095: Steralization Tray
• 07290109146904: Versacut Tissue Morcellator, MORCELLATOR WITH HOLEP TRAINING
• 07290109146850: VersaCut Tissue Morcellator Control Unit