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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
First aid limb splint, non-mouldable, reusable FDA UDI
Device Name
ECONO PADDED BOARD SPLINT, 42" FDA UDI
Model / Reference
1842 FDA UDI
Description
ECONO PADDED BOARD SPLINT, 42" FDA UDI

Identifiers

Catalog Number
1842 FDA UDI
Primary DI / UDI-DI
00647921184206 FDA UDI
FDA Product Code
NOC FDA UDI
GMDN Term
First aid limb splint, non-mouldable, 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: First aid limb splint, non-mouldable, reusable

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

Similar devices

Also classified as First aid limb splint, non-mouldable, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 60c68717-a4e1-4038-89ae-ff6206406f58 35 fields · synced May 30, 2026