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Electrolite

FDA UDI

Class II (US FDA UDI)

by Dermatologic Lab And Supply, Inc.

Identity

Trade Name
Electrolite FDA UDI
Generic Name
Open-surgery electrosurgical electrode, monopolar, single-use FDA UDI
Device Name
E, ELECTRODE, ELECTROLITE SAMPLE PACK OF 50. Medical device. FDA UDI
Model / Reference
26250 FDA UDI
Description
E, ELECTRODE, ELECTROLITE SAMPLE PACK OF 50. Medical device. FDA UDI

Identifiers

Primary DI / UDI-DI
10609960001248 FDA UDI
510(k) Number
K010025 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery electrosurgical electrode, monopolar, single-use

Electrolite by Dermatologic Lab And Supply, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical electrode, monopolar, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3193fa3e-222b-4c89-a634-4be2c9683b40 34 fields · synced May 30, 2026