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Spectra 360 Electrode Gel

FDA UDI

Class II (US FDA UDI)

by Axiobionics, LLC

Identity

Trade Name
Spectra 360 Electrode Gel FDA UDI
Generic Name
Electrode conductive medium FDA UDI
Device Name
Electrode Gel Monthly Supply (4 8 oz tubes) FDA UDI
Model / Reference
0 FDA UDI
Description
Electrode Gel Monthly Supply (4 8 oz tubes) FDA UDI

Identifiers

Catalog Number
145M FDA UDI
Primary DI / UDI-DI
B367145M00 FDA UDI
FDA Product Code
GYB FDA UDI
GMDN Term
Electrode conductive medium FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1275 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrode conductive medium

Spectra 360 Electrode Gel by Axiobionics, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrode conductive medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Axiobionics, LLC

Sources (1)

  • FDA UDI d0aaf32c-24e5-49d0-8d6f-685dbd491054 34 fields · synced May 30, 2026