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MedSource Stretcher

FDA UDI

Class I (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Stretcher FDA UDI
Generic Name
Ambulance stretcher, manual FDA UDI
Device Name
Stretcher, Folding, Burgundy FDA UDI
Model / Reference
MS-EFS123 FDA UDI
Description
Stretcher, Folding, Burgundy FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00816703029824 FDA UDI
FDA Product Code
FPP FDA UDI
GMDN Term
Ambulance stretcher, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6900 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: Ambulance stretcher, manual

MedSource Stretcher by Medsource International Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulance stretcher, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 896af379-ae05-4116-9d0d-d5620a7a7d67 34 fields · synced May 30, 2026