Dragonfly®

GUDID B006DCKITST1

NEUROVISION MEDICAL PRODUCTS, INC.

Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode Electromyographic endotracheal tube electrode

• Primary Device ID: B006DCKITST1
• NIH Device Record Key: 30af7298-e226-4a8a-8f3a-04d3772973db
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dragonfly®
• Version Model Number: N/A
• Company DUNS: 182057401
• Company Name: NEUROVISION MEDICAL PRODUCTS, INC.
• 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: 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
HIBCC	B006DCKITST1 [Unit of Use]
HIBCC	B006DCKITST52 [Primary]
HIBCC	DCKITST5 [Package]; Contains: B006DCKITST52; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• ETN: Stimulator, Nerve

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-28
• Device Publish Date: 2023-03-20

On-Brand Devices [Dragonfly®]

• B006DCKITLT1: N/A
• DCKITLD5: N/A
• B006LTE7003PLD1: N/A
• B006EAKITMT1: N/A
• B006EAKITMSPD1: N/A
• B006EAKITMSP1: N/A
• B006EAKITMD1: N/A
• B006EAKITM1: N/A
• B006DCKITST1: N/A
• B006DCKITSD1: N/A
• SCKITMT5: N/A
• SCKITMST5: N/A
• SCKITMSD5: N/A
• SCKITMS5: N/A
• SCKITMD5: N/A
• SCKITM5: N/A