eudamed_udi
Primary ID: 05904553993428
UV protected infusion set IS (UDI 05904553993428)
Manufactured by MARGOMED SPÓŁKA AKCYJNA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UV protected infusion set IS - Primary ID 05904553993428
Device Regulatory Overview
The UV protected infusion set IS (Model/Catalog Number: 001 482) is a medical device manufactured by MARGOMED SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification A03040199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 001 482
- Product Code / EMDN
- A03040199
- Device Name
- Infusion Set
- Database Sync Date
- 2026-08-09 16:59:47
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 UV protected infusion set IS?
The registered manufacturer of record for UV protected infusion set IS is MARGOMED SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for UV protected infusion set IS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904553993428.
What classification code is assigned to this device?
This device is registered under product classification code A03040199.
Similar Classification Devices (A03040199)
Other Devices by MARGOMED SPÓŁKA AKCYJNA
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