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Assembly Required Distributors

FDA UDI

Class I (US FDA UDI)

by Assembly Required Distributors Inc

Identity

Trade Name
Assembly Required Distributors FDA UDI
Generic Name
Infusion/transfusion trolley FDA UDI
Device Name
Arm Pad Cushion, black urethane FDA UDI
Model / Reference
IVM1920-01 FDA UDI
Description
Arm Pad Cushion, black urethane FDA UDI

Identifiers

Primary DI / UDI-DI
00854362008842 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Infusion/transfusion trolley FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Infusion/transfusion trolley

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

Similar devices

Also classified as Infusion/transfusion trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Assembly Required Distributors Inc

Sources (1)

  • FDA UDI 7a782237-97b8-47f6-9ec3-48e07233ec2d 33 fields · synced May 30, 2026