eudamed_udi
Primary ID: 50126542021008
Powerstep (UDI 50126542021008)
Manufactured by Cuxson Gerrard & Co. Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Powerstep - Primary ID 50126542021008
Device Regulatory Overview
The Powerstep (Model/Catalog Number: POW055) is a medical device manufactured by Cuxson Gerrard & Co. Ltd. This product is indexed under FDA Product Code / Category Classification Y061203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- POW055
- Product Code / EMDN
- Y061203
- Device Name
- Orthotics
- Database Sync Date
- 2026-08-09 16:49:17
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Powerstep?
The registered manufacturer of record for Powerstep is Cuxson Gerrard & Co. Ltd.
What is the Primary UDI-DI identifier for Powerstep?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50126542021008.
What classification code is assigned to this device?
This device is registered under product classification code Y061203.
Similar Classification Devices (Y061203)
Other Devices by Cuxson Gerrard & Co. Ltd
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