Scorpion

GUDID IDKMF512B5

NEUROVISION MEDICAL PRODUCTS, INC.

Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use Nerve-locating system probe, single-use

• Primary Device ID: IDKMF512B5
• NIH Device Record Key: 9093c963-d9c9-42c5-aa83-e2d114eb4750
• 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: 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B006IDKMF512B5 [Unit of Use]
HIBCC	B006IDKMF512B52 [Primary]
HIBCC	IDKMF512B5 [Package]; Contains: B006IDKMF512B52; Package: [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091410

FDA Product Code

• ETN: Stimulator, Nerve

Sterilization

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

[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

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[IDKMF512B5]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-25
• Device Publish Date: 2021-11-17

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