FOOT SWITCH

GUDID 08809502330033

VIOL Co.,Ltd.

Electrosurgical system

• Primary Device ID: 08809502330033
• NIH Device Record Key: cd22418a-c48c-4dae-b842-c3974dfbf61b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FOOT SWITCH
• Version Model Number: F/S
• Company DUNS: 695654949
• Company Name: VIOL Co.,Ltd.
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809502330033 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172023

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-01-15
• Device Publish Date: 2018-04-02

On-Brand Devices [FOOT SWITCH]

• 08809502330033: F/S
• 08809502330187: F/S-B