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MedSource Flex-All Splint

FDA UDI

Class I (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Flex-All Splint FDA UDI
Generic Name
First aid limb splint, mouldable, reusable FDA UDI
Device Name
Flex-all Splint, Black, No Fold, BULK FDA UDI
Model / Reference
MS-93001 FDA UDI
Description
Flex-all Splint, Black, No Fold, BULK FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00840155405820 FDA UDI
FDA Product Code
ILH FDA UDI
GMDN Term
First aid limb splint, mouldable, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: First aid limb splint, mouldable, reusable

MedSource Flex-All Splint by Medsource International Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a23c55e5-4682-4a7b-afb5-f2ba23d0c5d4 34 fields · synced May 31, 2026