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Morrison Medical

FDA UDI

Class I (US FDA UDI)

by Morrison Medical, Ltd

Identity

Trade Name
MORRISON MEDICAL FDA UDI
Generic Name
Armboard, reusable FDA UDI
Device Name
REUSABLE ARMBOARD,1X4 FDA UDI
Model / Reference
1032 FDA UDI
Description
REUSABLE ARMBOARD,1X4 FDA UDI

Identifiers

Catalog Number
1032 FDA UDI
Primary DI / UDI-DI
00647921103207 FDA UDI
FDA Product Code
NOD FDA UDI
GMDN Term
Armboard, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.3910 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Armboard, reusable

Morrison Medical by Morrison Medical, Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Armboard, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Morrison Medical, Ltd

Sources (1)

  • FDA UDI 2bcb9f18-240d-4acb-9f84-7c2cb522a998 35 fields · synced May 29, 2026