Disc-FX® System

GUDID 00846338000691

ELLIQUENCE, LLC

Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

• Primary Device ID: 00846338000691
• NIH Device Record Key: 18cc8c98-4ba6-4ce5-ad71-060c8113f0f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disc-FX® System
• Version Model Number: DFX
• Company DUNS: 019872358
• Company Name: ELLIQUENCE, LLC
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	00846338000691 [Primary]

FDA Product Code

• HRX: Arthroscope

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-04-23
• Device Publish Date: 2016-09-22

Devices Manufactured by ELLIQUENCE, LLC

• 00846338000776 - Spine Needle (18 Gauge): 2019-07-22
• 00846338000066 - Trigger-Flex®: 2019-04-23 S 36cm
• 00846338000288 - Trigger-Flex®: 2019-04-23
• 00846338000448 - Bi-Tip™ Flextrode™: 2019-04-23
• 00846338000455 - Trigger-Flex®: 2019-04-23
• 00846338000462 - Micro Bipolar: 2019-04-23
• 00846338000479 - Micro Bipolar: 2019-04-23
• 00846338000486 - Bi-Tip™ Flextrode™: 2019-04-23