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DeRoyal

FDA UDI

Class I (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name
DeRoyal FDA UDI
Generic Name
Shoulder immobilizer/orthosis, reusable FDA UDI
Device Name
Shoulder P.A.D. FDA UDI
Model / Reference
11640008-COSM FDA UDI
Description
Shoulder P.A.D. FDA UDI

Identifiers

Catalog Number
11640008-COSM FDA UDI
Primary DI / UDI-DI
00749756350976 FDA UDI
FDA Product Code
ILI FDA UDI
GMDN Term
Shoulder immobilizer/orthosis, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3640 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Shoulder immobilizer/orthosis, reusable

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

Similar devices

Also classified as Shoulder immobilizer/orthosis, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0c314313-effe-4a7a-8484-a3feedeaa278 35 fields · synced Jun 8, 2026