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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
Walking aid tip FDA UDI
Device Name
Doctor Stool Replacement Rubber Tip FDA UDI
Model / Reference
CHM8908-01 FDA UDI
Description
Doctor Stool Replacement Rubber Tip FDA UDI

Identifiers

Primary DI / UDI-DI
00860004575627 FDA UDI
FDA Product Code
INP FDA UDI
GMDN Term
Walking aid tip FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3790 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: Walking aid tip

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 Walking aid tip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b6a27381-20b2-4da1-ab2d-88a4856b76d8 33 fields · synced Jun 8, 2026