Probe

GUDID 00846338002190

ELLIQUENCE, LLC

Spinal endoscopic-access system

• Primary Device ID: 00846338002190
• NIH Device Record Key: d2e46a0b-38be-428a-b552-669ab4da2db2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Probe
• Version Model Number: 11-2415
• Company DUNS: 019872358
• Company Name: ELLIQUENCE, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846338002190 [Primary]

FDA Product Code

• HXB: Probe

Sterilization

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

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

[00846338002190]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-17
• Device Publish Date: 2025-01-09

On-Brand Devices [Probe]

• 00846338006839: 11-2426
• 00846338002213: 11-2413
• 00846338002206: 11-2420
• 00846338002190: 11-2415