Ikegami

GUDID 00886874110164

CAMERA HEAD VIDEO CABLE, IKEGAMI, HD

INTUITIVE SURGICAL, INC.

Electrical-only medical device connection cable, reusable

• Primary Device ID: 00886874110164
• NIH Device Record Key: 260b7b68-b7d2-45bf-b395-771107e0ca52
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ikegami
• Version Model Number: 370884
• 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 Dimensions

• Length: 43 Feet
• Length: 43 Feet

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886874110164 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050369

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: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-03-02
• Device Publish Date: 2016-07-08

Devices Manufactured by INTUITIVE SURGICAL, INC.

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• 00886874125502 - da Vinci 12mm Assist Cannula: 2025-08-28 CANNULA, STANDARD, REUSABLE, ASSIST
• 00886874125519 - Da Vinci 8mm Assist Cannula: 2025-08-28 CANNULA, STANDARD, REUSABLE, ASSIST
• 10886874123369 - da Vinci Energy: 2025-08-22 Vessel Sealer Curved
• 10886874124588 - None: 2025-07-16 None
• 00886874125588 - Force Feedback: 2025-07-01 Force Feedback Fenestrated Bipolar Forceps