ASG 120

GUDID 00815871020008

Avante

Electrosurgical system

• Primary Device ID: 00815871020008
• NIH Device Record Key: e3fdacb6-f5d5-4b54-8bea-2c13894fe5df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASG 120
• Version Model Number: 71250ASG
• Company DUNS: 178440426
• Company Name: Avante
• 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	00815871020008 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K001955

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: 4
• Public Version Date: 2019-06-19
• Device Publish Date: 2016-09-23

On-Brand Devices [ASG 120]

• 00815871020015: 71250ASGR
• 00815871020008: 71250ASG