Nerveana

GUDID B006NVTKITC3P81

NEUROVISION MEDICAL PRODUCTS, INC.

Electromyographic endotracheal tube

• Primary Device ID: B006NVTKITC3P81
• NIH Device Record Key: e9c95397-1852-402c-ad4b-1c890a2aa7a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nerveana
• 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: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B006NVTKITC3P81 [Unit of Use]
HIBCC	B006NVTKITC3P852 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110989

FDA Product Code

• GWF: Stimulator, Electrical, Evoked Response

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-08-20
• Device Publish Date: 2020-08-12

On-Brand Devices [Nerveana]

• B006NVTKITC3P81: N/A
• B006NVTKITC3P71: N/A
• B006NVTKITC3P61: N/A
• B006STTABLET2: N/A
• B006STRLP0: N/A
• B006SMBC0: N/A
• B006NV0060: N/A
• B006NRVTABLET0: N/A
• B006DSMBC52: N/A
• B006CSTIB260: N/A
• B006CEMGB60: N/A