Double Pedal Foot Switch

GUDID 04057607000182

KLS Martin GmbH + Co. KG

Foot-switch, electrical

• Primary Device ID: 04057607000182
• NIH Device Record Key: e1889444-058d-47e5-9ccc-e8823dbf5ce1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Double Pedal Foot Switch
• Version Model Number: CE200-A05
• Company DUNS: 340331859
• Company Name: KLS Martin GmbH + Co. KG
• 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	04057607000182 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081678

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: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [Double Pedal Foot Switch]

• 04057607000182: CE200-A05
• 04057607000168: CE200-A01