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Walking Aid

FDA UDI

Class I (US FDA UDI)

by Paramount Bed Co., Ltd.

Identity

Trade Name
Walking Aid FDA UDI
Generic Name
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI
Device Name
Walking Aid with brake. This device also provides IV pole to hold other medical devices. FDA UDI
Model / Reference
KA-392U FDA UDI
Description
Walking Aid with brake. This device also provides IV pole to hold other medical devices. FDA UDI

Identifiers

Primary DI / UDI-DI
04527799700028 FDA UDI
FDA Product Code
ITJ FDA UDI
FOX FDA UDI
GMDN Term
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3825 FDA UDI
880.6990 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: Handgrip disability-assistive walker, non-powered, non-foldable

Walking Aid by Paramount Bed Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Handgrip disability-assistive walker, non-powered, non-foldable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paramount Bed Co., Ltd.

Sources (1)

  • FDA UDI feb577da-9789-4c3c-8d98-044e3e15acbc 33 fields · synced Jun 8, 2026