Forceps

GUDID 00846338001391

ELLIQUENCE, LLC

Rigid endoscopic biopsy forceps, reusable

• Primary Device ID: 00846338001391
• NIH Device Record Key: 4c6ac7ef-a349-482c-bb49-c4156616d91c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Forceps
• Version Model Number: DFX-GS
• 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: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846338001391 [Primary]

FDA Product Code

• GEN: Forceps, General & Plastic Surgery

Sterilization

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

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

Moist Heat or Steam Sterilization

[00846338001391]

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 [Forceps]

• 00846338001391: DFX-GS
• 00846338000738: DFX-G