← Back to catalogue

Alpha-Stim

FDA UDI

Class II (US FDA UDI)

by Parker Laboratories, Inc.

Identity

Trade Name
Alpha-Stim FDA UDI
Generic Name
Electrode conductive medium FDA UDI
Device Name
Conducting Solution - 250 ml FDA UDI
Model / Reference
18-25-155614-1 FDA UDI
Description
Conducting Solution - 250 ml FDA UDI

Identifiers

Catalog Number
SL250 FDA UDI
Primary DI / UDI-DI
10855683006941 FDA UDI
510(k) Number
K780973 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrode conductive medium

Alpha-Stim by Parker Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrode conductive medium.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4a5d3a9d-f9d7-430a-a100-0c9955c6ccd1 36 fields · synced Jun 1, 2026