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Thermalite Disposable TCU Electrodes

FDA UDI

Class II (US FDA UDI)

by Dermatologic Lab And Supply, Inc.

Identity

Trade Name
Thermalite Disposable TCU Electrodes FDA UDI
Generic Name
Electrocautery system electrode FDA UDI
Device Name
THERMALITE DISPOSABLE TCU TIPS, LOOP, BOX OF 10. Medical Device. FDA UDI
Model / Reference
210T FDA UDI
Description
THERMALITE DISPOSABLE TCU TIPS, LOOP, BOX OF 10. Medical Device. FDA UDI

Identifiers

Catalog Number
210T FDA UDI
Primary DI / UDI-DI
10609960000999 FDA UDI
FDA Product Code
HQO FDA UDI
GMDN Term
Electrocautery system electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4115 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

Yes

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: Electrocautery system electrode

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

Similar devices

Also classified as Electrocautery system electrode.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dermatologic Lab And Supply, Inc.

Sources (1)

  • FDA UDI 86598f66-4f46-41b0-91e0-2410dae944b7 34 fields · synced Jun 8, 2026