da Vinci Energy

GUDID 00886874120880

E-200 Generator

INTUITIVE SURGICAL, INC.

Electrosurgical system generator

• Primary Device ID: 00886874120880
• NIH Device Record Key: a26efdf0-e950-4f0b-b266-80f04f383a13
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: da Vinci Energy
• Version Model Number: 378897
• Company DUNS: 938647021
• Company Name: INTUITIVE SURGICAL, 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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	00886874120880 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223039

FDA Product Code

• GEI: Electrosurgical, cutting & coagulation & accessories

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: 2023-11-23
• Device Publish Date: 2023-11-15

On-Brand Devices [da Vinci Energy]

• 10886874117306: SynchroSeal
• 00886874116982: E-100 Generator
• 00886874123867: E-200 Gen 4 Generator Upgrade
• 00886874120880: E-200 Generator
• 00886874124000: Da Vinci Monopolar and Bipolar Adapters