Versacut™ GA-0000200

GUDID 07290109146904

Versacut Tissue Morcellator, MORCELLATOR WITH HOLEP TRAINING

LUMENIS LTD.

Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system Tissue morcellation system

• Primary Device ID: 07290109146904
• NIH Device Record Key: 2cc6ed89-715f-48c1-8587-ba04e1a691ec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Versacut™
• Version Model Number: Versacut™
• Catalog Number: GA-0000200
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109146904 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-12
• Device Publish Date: 2022-09-04

On-Brand Devices [Versacut™]

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