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Walkasins

FDA UDI

Class II (US FDA UDI)

by Rxfunction Inc.

Identity

Trade Name
Walkasins FDA UDI
Generic Name
Dynamic-response foot prosthesis FDA UDI
Device Name
System, Large FDA UDI
Model / Reference
W-100 FDA UDI
Description
System, Large FDA UDI

Identifiers

Catalog Number
W-100-02 FDA UDI
Primary DI / UDI-DI
00850004761052 FDA UDI
FDA Product Code
ISW FDA UDI
GMDN Term
Dynamic-response foot prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3500 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

Yes

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

Yes

FDA UDI

Category: Dynamic-response foot prosthesis

Walkasins by Rxfunction Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dynamic-response foot prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rxfunction Inc.

Sources (1)

  • FDA UDI b974128f-6c99-4988-9abf-3e1790dd2568 35 fields · synced Jun 8, 2026