eudamed_udi
Primary ID: 05020581265112
Unspecified Brand (UDI 05020581265112)
Manufactured by Steroplast Healthcare Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 05020581265112
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 9500) is a medical device manufactured by Steroplast Healthcare Ltd. This product is indexed under FDA Product Code / Category Classification M0304010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9500
- Product Code / EMDN
- M0304010102
- Device Name
- Joint Supports
- Database Sync Date
- 2026-08-09 16:46:10
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Steroplast Healthcare Ltd.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05020581265112.
What classification code is assigned to this device?
This device is registered under product classification code M0304010102.
Similar Classification Devices (M0304010102)
Other Devices by Steroplast Healthcare Ltd
Programmatic Export
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