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Sliding Board, 8X30

FDA UDI

Class I (US FDA UDI)

by Hausmann Enterprises, Llc

Identity

Trade Name
Sliding Board,8X30 FDA UDI
Generic Name
Wheelchair lap tray FDA UDI
Model / Reference
5089 FDA UDI

Identifiers

Primary DI / UDI-DI
00840314801630 FDA UDI
FDA Product Code
IMX FDA UDI
GMDN Term
Wheelchair lap tray 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair lap tray

Sliding Board, 8X30 by Hausmann Enterprises, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair lap tray.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 89ea326b-3f7e-4f34-a1ab-d0d1e1023b63 32 fields · synced May 30, 2026