da Vinci SP

GUDID 00886874114605

PATIENT SIDE CART

INTUITIVE SURGICAL, INC.

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• Primary Device ID: 00886874114605
• NIH Device Record Key: cba189c8-b670-4ffd-8b39-87c399fe7d87
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: da Vinci SP
• Version Model Number: 380601
• 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	00886874114605 [Primary]

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: 2020-09-16
• Device Publish Date: 2020-09-08

On-Brand Devices [da Vinci SP]

• 00886874114742: VISION SYSTEM CART
• 00886874114735: SURGEON SIDE CONSOLE
• 00886874114605: PATIENT SIDE CART