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DeRoyal

FDA UDI

Class I (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name
DeRoyal FDA UDI
Generic Name
Wheelchair/chair/stander occupant restraint/support FDA UDI
Device Name
HOLDER FOR FDA UDI
Model / Reference
M2815D01 FDA UDI
Description
HOLDER FOR FDA UDI

Identifiers

Catalog Number
M2815D01 FDA UDI
Primary DI / UDI-DI
00749756112345 FDA UDI
FDA Product Code
KID FDA UDI
GMDN Term
Wheelchair/chair/stander occupant restraint/support FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3910 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Wheelchair/chair/stander occupant restraint/support

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

Similar devices

Also classified as Wheelchair/chair/stander occupant restraint/support.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5742c4b2-876b-4f5e-90b5-4c536c2f1266 35 fields · synced Jun 8, 2026