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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-USA FDA UDI
Model / Reference
MS-SPLINT-2 FDA UDI
Description
Flex-all Splint-USA FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00816703027455 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

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

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 is a portable, mouldable, and reusable first aid limb splint designed for emergency immobilization of injured extremities. It features a semi-rigid, padded, metallic sheet or wire frame that can be manually moulded around the limb to create a rigid splint. This device is intended for use by EMS personnel and is available in a single-use package with 100 units per case.

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

Manufacturer
Medsource International Llc

Sources (1)

  • FDA UDI 82771cbc-af08-464f-856e-64f5bd2e21a2 34 fields · synced Jul 31, 2026