Scorpion

GUDID B006IATF714BL0

NEUROVISION MEDICAL PRODUCTS, INC.

Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating probe, reusable Nerve-locating system probe, reusable Nerve-locating system probe, reusable Nerve-locating system probe, reusable Nerve-locating system probe, reusable Nerve-locating system probe, reusable Nerve-locating system probe, reusable Nerve-locating system probe, reusable Nerve-locating system probe, reusable Nerve-locating system probe, reusable

• Primary Device ID: B006IATF714BL0
• NIH Device Record Key: 0535def0-a55a-4293-af37-d0e3788c54c7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Scorpion
• Version Model Number: N/A
• Company DUNS: 182057401
• Company Name: NEUROVISION MEDICAL PRODUCTS, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	B006IATF714BL0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121931

FDA Product Code

• ETN: Stimulator, Nerve

Sterilization

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

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

[B006IATF714BL0]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-01-05
• Device Publish Date: 2020-12-28

On-Brand Devices [Scorpion]

• B006T61075D0: N/A
• B006ICSI0: N/A
• B006IATF714BL0: N/A
• B006IATF714B0: N/A
• IDKMF512B5: N/A
• IDKATF714B5: N/A
• IDKWSF5125: N/A