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Brevio

FDA UDI

Class II (US FDA UDI)

by Neurotron Medical, Inc.

Identity

Trade Name
Brevio FDA UDI
Generic Name
Diagnostic peripheral nerve electrical stimulation system FDA UDI
Device Name
Neuro-sensor, 5 pouches/box FDA UDI
Model / Reference
BRV-0250 FDA UDI
Description
Neuro-sensor, 5 pouches/box FDA UDI

Identifiers

Primary DI / UDI-DI
B1870223 FDA UDI
510(k) Number
K012069 FDA UDI
FDA Product Code
JXE FDA UDI
GMDN Term
Diagnostic peripheral nerve electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1550 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Diagnostic peripheral nerve electrical stimulation system

Brevio by Neurotron Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diagnostic peripheral nerve electrical stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neurotron Medical, Inc.

Sources (1)

  • FDA UDI a0e54f0c-f1ec-4c3d-aca6-7d0ef24c58c5 34 fields · synced Jun 1, 2026