gudid
Primary ID: LiteWalk
LiteWalk (UDI LiteWalk)
Manufactured by VIASONIX LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LiteWalk - Primary ID LiteWalk
Device Regulatory Overview
The LiteWalk (Model/Catalog Number: LiteWalk) is a medical device manufactured by VIASONIX LTD. This product is indexed under FDA Product Code / Category Classification IRP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LiteWalk
- Product Code / EMDN
- IRP
- Device Name
- The LiteWalk is Intended for home and hospital use for temporary increase in local blood circulation in the lower extremities and temporary relief of minor muscle aches and pains where applied. The system is based on a pneumatic unit that includes a pump, valves, pressure sensor and tubing, and is fed by an external power supply of 12V DC. The LiteWalk doesn't contains a software user interface. The 2 sandals (right/left) are inflated together at the same time with the same pump. The inflation cycle is sequential, as follows: inflate heel, inflate arch, deflate heel, inflate metatarsals, deflate arch, inflate toes, deflate metatarsals, deflate toes
- Database Sync Date
- 2026-08-09 09:18:18
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of LiteWalk?
The registered manufacturer of record for LiteWalk is VIASONIX LTD.
What is the Primary UDI-DI identifier for LiteWalk?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LiteWalk.
What classification code is assigned to this device?
This device is registered under product classification code IRP.
Similar Classification Devices (IRP)
Other Devices by VIASONIX LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint