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Geiger TCU Cautery Sheath

FDA UDI

Class II (US FDA UDI)

by Dermatologic Lab And Supply, Inc.

Identity

Trade Name
Geiger TCU Cautery Sheath FDA UDI
Generic Name
Instrument/equipment drape, single-use, non-sterile FDA UDI
Device Name
TCU, CAUTERY SHEATH, NONSTERILE, BOX OF 100. Medical Device. FDA UDI
Model / Reference
220 FDA UDI
Description
TCU, CAUTERY SHEATH, NONSTERILE, BOX OF 100. Medical Device. FDA UDI

Identifiers

Catalog Number
220 FDA UDI
Primary DI / UDI-DI
10609960000852 FDA UDI
FDA Product Code
HQO FDA UDI
GMDN Term
Instrument/equipment drape, single-use, non-sterile 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

Category: Instrument/equipment drape, single-use, non-sterile

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

Similar devices

Also classified as Instrument/equipment drape, single-use, non-sterile.

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 bf7008d6-a38c-4b69-909d-f2bb413b4954 34 fields · synced Jun 1, 2026