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Alpha Conducting Solution

FDA UDI

Class III (US FDA UDI)

by Electromedical Products International, Inc.

Identity

Trade Name
Alpha Conducting Solution FDA UDI
Generic Name
Electrode conductive medium FDA UDI
Device Name
Alpha Conducting Solution Refill 250ml FDA UDI
Model / Reference
ACSR FDA UDI
Description
Alpha Conducting Solution Refill 250ml FDA UDI

Identifiers

Primary DI / UDI-DI
00857869005086 FDA UDI
FDA Product Code
JXK FDA UDI
GMDN Term
Electrode conductive medium FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
882.5800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Alpha Conducting Solution by Electromedical Products International, Inc. — Class III — 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

Sources (1)

  • FDA UDI 7a9a402b-921f-4e13-8a72-fd005532887e 33 fields · synced May 30, 2026