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Geiger Thermal Cautery Unit

FDA UDI

Class II (US FDA UDI)

by Dermatologic Lab And Supply, Inc.

Identity

Trade Name
Geiger Thermal Cautery Unit FDA UDI
Generic Name
Electrocautery system generator, line-powered FDA UDI
Device Name
TCU, THERMAL CAUTERY, UNIT ONLY, 220v. Medical Device. FDA UDI
Model / Reference
150A FDA UDI
Description
TCU, THERMAL CAUTERY, UNIT ONLY, 220v. Medical Device. FDA UDI

Identifiers

Catalog Number
150A FDA UDI
Primary DI / UDI-DI
00609960001128 FDA UDI
510(k) Number
K002341 FDA UDI
FDA Product Code
HQO FDA UDI
GMDN Term
Electrocautery system generator, line-powered 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocautery system generator, line-powered

Geiger Thermal Cautery Unit 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 generator, line-powered.

Cleared under the same submission

K002341 also covers:

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 dc26f1ae-29e0-4687-906c-73c2e5315208 35 fields · synced Jun 6, 2026