Force Feedback

GUDID 10886874120740

Force Feedback Fenestrated Bipolar Forceps

INTUITIVE SURGICAL, INC.

Robotic electrosurgical instrument, bipolar, reusable

• Primary Device ID: 10886874120740
• NIH Device Record Key: 5c6f937b-4acd-4d02-8529-2349b2b813d9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Force Feedback
• Version Model Number: 475205
• 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: true
• Serial Number: false
• 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

• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter
• Outer Diameter: 8 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886874120743 [Primary]
GS1	10886874120740 [Package]; Contains: 00886874120743; Package: BOX [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232610

FDA Product Code

• NAY: System, surgical, computer controlled instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

[10886874120740]

Moist Heat or Steam Sterilization

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 [Force Feedback]

• 10886874120757: Force Feedback Mega SutureCut Needle Driver
• 10886874120740: Force Feedback Fenestrated Bipolar Forceps
• 10886874120733: Force Feedback Maryland Bipolar Forceps
• 10886874120726: Force Feedback ProGrasp Forceps
• 10886874120719: Force Feedback Cadiere Forceps
• 10886874120702: Force Feedback Large Needle Driver
• 00886874125458: Force Feedback Mega SutureCut Needle Driver
• 00886874125434: Force Feedback ProGrasp Forceps