← Back to catalogue

DeRoyal

FDA UDI

Class I (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name
DeRoyal FDA UDI
Generic Name
Surgical towel FDA UDI
Device Name
O.R Towel, X-Ray Detectable FDA UDI
Model / Reference
68-402 FDA UDI
Description
O.R Towel, X-Ray Detectable FDA UDI

Identifiers

Catalog Number
68-402 FDA UDI
Primary DI / UDI-DI
00749756173803 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Surgical towel 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical towel

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

Similar devices

Also classified as Surgical towel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI d5694855-e962-4db9-9aa8-d9f277d0c300 35 fields · synced Jun 6, 2026