Geiger TCU Handpiece

FDA UDI

Class II (US FDA UDI)

by Dermatologic Lab And Supply, Inc.

Identity

Trade Name: Geiger TCU Handpiece FDA UDI
Generic Name: Electrocautery system handpiece FDA UDI
Device Name: CAUTERY HANDPIECE, REPLACEMENT, FOR GEIGER TCU. Medical Device. FDA UDI
Model / Reference: 250 FDA UDI
Description: CAUTERY HANDPIECE, REPLACEMENT, FOR GEIGER TCU. Medical Device. FDA UDI

Identifiers

Catalog Number: 250 FDA UDI
Primary DI / UDI-DI: 00609960000824 FDA UDI
FDA Product Code: HQO FDA UDI
GMDN Term: Electrocautery system handpiece 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Electrocautery system handpiece

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Dermatologic Lab And Supply, Inc.

Sources (1)

FDA UDI 452174a0-6377-4d81-a5eb-b338d1a647c3 34 fields · synced Jun 8, 2026