Clear-Vu® Bayonet Electrode

GUDID 00846338000578

ELLIQUENCE, LLC

Open-surgery electrosurgical electrode, monopolar, single-use

• Primary Device ID: 00846338000578
• NIH Device Record Key: 440a0193-4842-4fb2-a582-ad44833122eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Clear-Vu® Bayonet Electrode
• Version Model Number: CV-N
• 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	00846338000578 [Primary]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2019-02-07
• Device Publish Date: 2016-09-22

On-Brand Devices [Clear-Vu® Bayonet Electrode]

• 00846338007980: CV-S/S
• 00846338007973: CV-N/S
• 00846338007966: CV-L7/S
• 00846338007959: CV-L5/S
• 00846338007942: CV-L3/S
• 00846338007935: CV-D/S
• 00846338007928: CV-B3/S
• 00846338007911: CV-B2/S
• 00846338000608: CV-W/S
• 00846338000592: CV-W
• 00846338000585: CV-S
• 00846338000578: CV-N
• 00846338000561: CV-L7
• 00846338000554: CV-L5
• 00846338000547: CV-L3
• 00846338000530: CV-D
• 00846338000523: CV-B3
• 00846338000516: CV-B2
• 00846338000509: CV-B1
• 00846338000394: CV-B1/S