Endiscope

GUDID 00846338001551

ELLIQUENCE, LLC

Diskectomy system, percutaneous, automatic

• Primary Device ID: 00846338001551
• NIH Device Record Key: a3976567-a307-4d04-84a4-7d8045104f6d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Endiscope
• Version Model Number: 10-2021
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• 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	00846338001551 [Primary]

FDA Product Code

• HRX: Arthroscope

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-08-27
• Device Publish Date: 2018-07-26

On-Brand Devices [Endiscope]

• 00846338001636: 10-2023
• 00846338001599: 10-2022
• 00846338001551: 10-2021
• 00846338001544: 10-2020