DeRoyal

FDA UDI

Class II (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name: DeRoyal FDA UDI
Generic Name: Surgical vessel loop FDA UDI
Device Name: Vessel Loops X-Ray Detectable FDA UDI
Model / Reference: 30-722L FDA UDI
Description: Vessel Loops X-Ray Detectable FDA UDI

Identifiers

Primary DI / UDI-DI: 00749756595438 FDA UDI
FDA Product Code: DXC FDA UDI
GMDN Term: Surgical vessel loop FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.4450 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

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Surgical vessel loop

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

Similar devices

Also classified as Surgical vessel loop.

Key Surgical Vascular Loops — Key Surgical, LLC · Class I
Wexler Surgical, Inc. — Wexler Surgical, Inc. · Class I
Devon — Cardinal Health 200, LLC · Class I
Degania — DEGANIA SILICONE LTD · Class II
Devon — Cardinal Health 200, LLC · Class I
Scanlan® SURG-I-LOOP® silicone loops — SCANLAN INTERNATIONAL INC · Class I
Sterion® Vessel Loop — Aspen Surgical Products, Inc. · Class I
Scanlan® SURG-I-LOOP® silicone loops — SCANLAN INTERNATIONAL INC · Class I

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

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Manufacturer

Manufacturer: Deroyal Industries, Inc.

Sources (1)

FDA UDI 0e7ca081-8e64-4e7c-9b50-239a8e6d6eb5 34 fields · synced Jun 8, 2026