Nerveäna+®

GUDID NVPTKITDCLWF5

NEUROVISION MEDICAL PRODUCTS, INC.

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• Primary Device ID: NVPTKITDCLWF5
• NIH Device Record Key: 1985cf48-ecfe-42fe-a666-049fcd9f43b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nerveäna+®
• Version Model Number: NONE
• 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	B006NVPTKITDCLWF5 [Unit of Use]
HIBCC	B006NVPTKITDCLWF52 [Primary]
HIBCC	NVPTKITDCLWF5 [Package]; Contains: B006NVPTKITDCLWF52; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• IKT: Electrode, Needle, Diagnostic Electromyograph

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: 2024-02-09
• Device Publish Date: 2024-02-01

On-Brand Devices [Nerveäna+®]

• NVPIC6: NONE
• NVPFKITMFT5: NONE
• NVPFKITMF5: NONE
• NVPFKITMDT5: NONE
• NVPFKITMD5: NONE
• NVPTKITDCST5: N/A
• NVPTKITDCS5: N/A
• NVPTKITDCLT5: N/A
• NVPTKITDCL5: N/A
• NVPTKITC3P8T5: N/A
• NVPTKITC3P85: N/A
• NVPTKITC3P7T5: N/A
• NVPTKITC3P75: N/A
• NVPTKITC3P6T5: N/A
• NVPTKITC3P65: N/A
• B006NVPTST2: N/A
• B600NVPS2: NONE
• B600NVPMS2: NONE
• B006NVPUSB1: NONE
• NVPTKITDCSWF5: NONE
• NVPTKITDCSD5: N/A
• NVPTKITDCLWF5: NONE
• NVPTKITDCLD5: N/A
• NVPTKITC3P8WSF5: N/A
• NVPTKITC3P7WSF5: N/A
• B006NVPTKITC3P6WSF5: N/A
• B006NVPT1: NONE
• B006NVPSTST2: NONE
• B006NVPMK1: NONE