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MedSource Vacuum Splint Set

FDA UDI

Class I (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Vacuum Splint Set FDA UDI
Generic Name
First aid limb splint, non-mouldable, reusable FDA UDI
Device Name
Vacuum Splint Set FDA UDI
Model / Reference
MS-DES FDA UDI
Description
Vacuum Splint Set FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00840155404069 FDA UDI
FDA Product Code
ILH FDA UDI
GMDN Term
First aid limb splint, non-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, non-mouldable, reusable

MedSource Vacuum Splint Set 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, non-mouldable, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2228c1e8-025b-4648-8d24-a3445bc26d1f 34 fields · synced May 30, 2026