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Assembly Required Distributors Inc.

FDA UDI

Class I (US FDA UDI)

by Assembly Required Distributors Inc

Identity

Trade Name
Assembly Required Distributors Inc. FDA UDI
Generic Name
Wheelchair antitip device FDA UDI
Device Name
Rear Anti-Tippers, MRI style with rubber tips, 4 holes and double push button pin FDA UDI
Model / Reference
AC1507-01 FDA UDI
Description
Rear Anti-Tippers, MRI style with rubber tips, 4 holes and double push button pin FDA UDI

Identifiers

Primary DI / UDI-DI
00860004575641 FDA UDI
FDA Product Code
IMR FDA UDI
GMDN Term
Wheelchair antitip device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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: Wheelchair antitip device

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

Similar devices

Also classified as Wheelchair antitip device.

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 dfa72199-ccc8-4290-8971-850e62fb8e37 33 fields · synced May 30, 2026