daVinci 5

GUDID 00886874119716

Patient Side Cart

INTUITIVE SURGICAL, INC.

Robotic surgical arm system

• Primary Device ID: 00886874119716
• NIH Device Record Key: 75f6d2f0-a600-45d0-a39c-fd6b4cd77b7f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: daVinci 5
• Version Model Number: 380747
• 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	00886874119716 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232610

FDA Product Code

• NAY: System, surgical, computer controlled instrument

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: 2024-03-29
• Device Publish Date: 2024-03-21

On-Brand Devices [daVinci 5]

• 00886874119747: Surgeon Side Cart
• 00886874119716: Patient Side Cart
• 00886874119662: Vision Side Cart
• 00886874124017: CO2 Supply Tank Interface Device
• 00886874123997: BLUE SYSTEM CABLE