Bipolar Forceps

GUDID 00846338002039

ELLIQUENCE, LLC

Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

• Primary Device ID: 00846338002039
• NIH Device Record Key: af2e146d-d1c1-4220-a0f6-b0c167a8b643
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bipolar Forceps
• Version Model Number: J7
• 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: 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	00846338002039 [Primary]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

[00846338002039]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-22

On-Brand Devices [Bipolar Forceps]

• 00846338002053: J7U
• 00846338002046: J7D
• 00846338002039: J7
• 00846338001995: J21
• 00846338001988: J20
• 00846338001940: J18
• 00846338001933: J17