H-Series Loop Electrode

GUDID GYNX1320101

GYNEX CORPORATION

Electrocautery system electrode

• Primary Device ID: GYNX1320101
• NIH Device Record Key: a0712d4b-f318-4773-812f-d60a1e8b7b01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: H-Series Loop Electrode
• Version Model Number: 13-2010
• Company DUNS: 012997685
• Company Name: GYNEX CORPORATION
• Device Count: 5
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	GYNX1320100 [Unit of Use]
HIBCC	GYNX1320101 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K982739

FDA Product Code

• HGI: Electrocautery, Gynecologic (And 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: 2018-07-06
• Device Publish Date: 2016-10-04

Devices Manufactured by GYNEX CORPORATION

• GYNX16000 - Gynex: 2024-01-03
• GYNX291000 - Gynex: 2024-01-03
• GYNX292000 - Gynex: 2024-01-03
• GYNX293500 - Gynex: 2024-01-03
• GYNX295500 - Gynex: 2024-01-03
• GYNX297000 - Gynex: 2024-01-03
• GYNX298000 - Gynex: 2024-01-03
• GYNX298500 - Gynex: 2024-01-03