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Axiom

FDA UDI

Class I (US FDA UDI)

by Ki Mobility, Llc

Identity

Trade Name
Axiom FDA UDI
Generic Name
Wheelchair head/trunk support, prefabricated FDA UDI
Device Name
4 x 5 Lateral Pads with Fixed Mounting Hardware for BTX - Right (E0956) FDA UDI
Model / Reference
Lateral Trunk Supports FDA UDI
Description
4 x 5 Lateral Pads with Fixed Mounting Hardware for BTX - Right (E0956) FDA UDI

Identifiers

Catalog Number
PBLF4X5PBR FDA UDI
Primary DI / UDI-DI
00840363368412 FDA UDI
FDA Product Code
KNO FDA UDI
GMDN Term
Wheelchair head/trunk support, prefabricated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3910 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

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 4 Inch FDA UDI
Width — 5 Inch FDA UDI

Category: Wheelchair head/trunk support, prefabricated

Axiom by Ki Mobility, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair head/trunk support, prefabricated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ki Mobility, Llc

Sources (1)

  • FDA UDI 49c58d5d-fb15-4f37-859e-33e52dd2e549 36 fields · synced Jun 1, 2026