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Scorpion

FDA UDI

Class II (US FDA UDI)

by Neurovision Medical Products, Inc.

Identity

Trade Name
Scorpion FDA UDI
Generic Name
Nerve-locating system probe, reusable FDA UDI
Model / Reference
N/A FDA UDI

Identifiers

Primary DI / UDI-DI
B006ICSI0 FDA UDI
510(k) Number
K121931 FDA UDI
FDA Product Code
ETN FDA UDI
GMDN Term
Nerve-locating system probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Nerve-locating system probe, reusable

Scorpion by Neurovision Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nerve-locating system probe, reusable.

Cleared under the same submission

K121931 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neurovision Medical Products, Inc.

Sources (1)

  • FDA UDI f5e9e26d-4c1f-4f8f-b90d-e8045b8790fe 33 fields · synced May 31, 2026