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Assembly Required Distributors

FDA UDI

Class II (US FDA UDI)

by Assembly Required Distributors Inc

Identity

Trade Name
Assembly Required Distributors FDA UDI
Generic Name
Hospital stretcher, manual FDA UDI
Device Name
Aluminum folding stretcher less pad, with 5" non ferrous casters, frame cut style 500lb. capacity. FDA UDI
Model / Reference
STA5011-01 FDA UDI
Description
Aluminum folding stretcher less pad, with 5" non ferrous casters, frame cut style 500lb. capacity. FDA UDI

Identifiers

Primary DI / UDI-DI
00865602000397 FDA UDI
FDA Product Code
FPO FDA UDI
GMDN Term
Hospital stretcher, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6910 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Hospital stretcher, manual

Assembly Required Distributors by Assembly Required Distributors Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hospital stretcher, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 19d5fe17-a5df-4cc4-ae61-6db0911e4134 33 fields · synced May 30, 2026