Dukal

FDA UDI

Class I (US FDA UDI)

by Dukal LLC

Identity

Trade Name: Dukal FDA UDI
Generic Name: Dry medical towel/wipe, single-use FDA UDI
Device Name: DK OR TowelCSR WrapSoftpack,ST16"x26"Green FDA UDI
Model / Reference: CT-04G FDA UDI
Description: DK OR TowelCSR WrapSoftpack,ST16"x26"Green FDA UDI

Identifiers

Catalog Number: CT-04G FDA UDI
Primary DI / UDI-DI: 00665973000459 FDA UDI
FDA Product Code: FRL FDA UDI
GMDN Term: Dry medical towel/wipe, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5300 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

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

Category: Dry medical towel/wipe, single-use

Dukal by Dukal LLC — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Dukal LLC

Sources (1)

FDA UDI c1cbf47f-4fe3-4fe9-a1f2-13fef85ebfc7 35 fields · synced Jun 1, 2026