Drive

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name: Drive FDA UDI
Generic Name: Wheelchair armrest FDA UDI
Device Name: ArmpadForNRS185006/7, 1/ea FDA UDI
Model / Reference: NRS185006-04 FDA UDI
Description: ArmpadForNRS185006/7, 1/ea FDA UDI

Identifiers

Primary DI / UDI-DI: 00822383505756 FDA UDI
FDA Product Code: KMN FDA UDI
GMDN Term: Wheelchair armrest FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6140 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Wheelchair armrest

Drive by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Hand Pad Horn Type — Otto Bock Mobility Solutions GmbH · Class I
Kit for nut-modular armrest — Otto Bock Mobility Solutions GmbH · Class I
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Drive Devilbiss Healthcare

Sources (1)

FDA UDI f261f770-5db8-4f17-971d-b6d24b4f0e6e 33 fields · synced Jun 8, 2026