DeRoyal

FDA UDI

Class II (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name: DeRoyal FDA UDI
Generic Name: Dry medical towel/wipe, single-use FDA UDI
Device Name: Blue OR Towels Bulk FDA UDI
Model / Reference: 63-001 FDA UDI
Description: Blue OR Towels Bulk FDA UDI

Identifiers

Primary DI / UDI-DI: 00749756024495 FDA UDI
FDA Product Code: PUI FDA UDI
GMDN Term: Dry medical towel/wipe, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4370 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dry medical towel/wipe, single-use

DeRoyal by Deroyal Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dry medical towel/wipe, single-use.

Medline — MEDLINE INDUSTRIES, INC. · Class II
Dukal — Dukal LLC · Class I
Bosma Enterprises — Bosma Enterprises · Class I
Tally Surgical Solution — TALLY SURGICAL, INC. · Class I
Medline — MEDLINE INDUSTRIES, INC. · Class II
AMD-RITMED — AMD Medicom Inc · Class I
Medical Action Industries — MEDICAL ACTION INDUSTRIES INC. · Class II
Medical Action Industries — MEDICAL ACTION INDUSTRIES INC. · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Deroyal Industries, Inc.

Sources (1)

FDA UDI daa3d30d-7396-4a06-9e83-3ada3d945cb2 34 fields · synced Jun 8, 2026