eudamed_udi
Primary ID: 03800728495013
Sterimed Fix (UDI 03800728495013)
Manufactured by Sopharma AD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sterimed Fix - Primary ID 03800728495013
Device Regulatory Overview
The Sterimed Fix (Model/Catalog Number: 32001000-0076) is a medical device manufactured by Sopharma AD. This product is indexed under FDA Product Code / Category Classification M04010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 32001000-0076
- Product Code / EMDN
- M04010101
- Device Name
- Sterimed - Sterile Wound Dressing
- Database Sync Date
- 2026-08-09 16:30:07
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 Sterimed Fix?
The registered manufacturer of record for Sterimed Fix is Sopharma AD.
What is the Primary UDI-DI identifier for Sterimed Fix?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03800728495013.
What classification code is assigned to this device?
This device is registered under product classification code M04010101.
Similar Classification Devices (M04010101)
Other Devices by Sopharma AD
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