eudamed_udi
Primary ID: 05904553993503
Infusion set IS PREMIUM (UDI 05904553993503)
Manufactured by MARGOMED SPÓŁKA AKCYJNA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Infusion set IS PREMIUM - Primary ID 05904553993503
Device Regulatory Overview
The Infusion set IS PREMIUM (Model/Catalog Number: 001 911P) 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 911P
- Product Code / EMDN
- A03040199
- Device Name
- Infusion Set
- Database Sync Date
- 2026-08-09 16:28:47
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 Infusion set IS PREMIUM?
The registered manufacturer of record for Infusion set IS PREMIUM is MARGOMED SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for Infusion set IS PREMIUM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904553993503.
What classification code is assigned to this device?
This device is registered under product classification code A03040199.
Similar Classification Devices (A03040199)
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