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Kit for nut-modular armrest

FDA UDI

Class I (US FDA UDI)

by Otto Bock Mobility Solutions GmbH

Identity

Trade Name
Kit for nut-modular armrest FDA UDI
Generic Name
Wheelchair armrest FDA UDI
Model / Reference
437A40 FDA UDI

Identifiers

Primary DI / UDI-DI
04032767350711 FDA UDI
FDA Product Code
KNN FDA UDI
GMDN Term
Wheelchair armrest 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

Category: Wheelchair armrest

Kit for nut-modular armrest by Otto Bock Mobility Solutions GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair armrest.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 91179cbd-bf8c-4c51-99d0-9a81b45cf329 32 fields · synced May 30, 2026