Cobra®

GUDID B006LTE7003PMD1

NEUROVISION MEDICAL PRODUCTS, INC.

Electromyographic endotracheal tube

• Primary Device ID: B006LTE7003PMD1
• NIH Device Record Key: c196d9ea-6c7a-44d1-b673-fa09db784e2d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cobra®
• 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	B006LTE7003PMD1 [Unit of Use]
HIBCC	B006LTE7003PMD52 [Primary]
HIBCC	LTE7003PMD5 [Package]; Contains: B006LTE7003PMD52; 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: 2023-04-14
• Device Publish Date: 2023-04-06

On-Brand Devices [Cobra®]

• LTE7003PSD5: N/A
• B006LTE7003PMD1: N/A