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DuraClip Hardware

FDA UDI

Class I (US FDA UDI)

by Motion Concepts Inc

Identity

Trade Name
DuraClip Hardware FDA UDI
Generic Name
Wheelchair back rest positioner FDA UDI
Device Name
DuraClip hardware (pair) for use with Matrx-Vi and Matrx Kidabra-Vi Base Cushions. Lock/release design used to secure the drop hook hardware to the seat fame. FDA UDI
Model / Reference
BDC FDA UDI
Description
DuraClip hardware (pair) for use with Matrx-Vi and Matrx Kidabra-Vi Base Cushions. Lock/release design used to secure the drop hook hardware to the seat fame. FDA UDI

Identifiers

Catalog Number
BDC FDA UDI
Primary DI / UDI-DI
07540147000585 FDA UDI
FDA Product Code
KNN FDA UDI
GMDN Term
Wheelchair back rest positioner 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

Yes

FDA UDI

Category: Wheelchair back rest positioner

DuraClip Hardware by Motion Concepts Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair back rest positioner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Motion Concepts Inc

Sources (1)

  • FDA UDI e9c42808-fb38-4c7b-9209-6df40ceda162 35 fields · synced May 30, 2026