Infusion set IS PREMIUM with injection site (UDI 05904553993558)
Manufactured by MARGOMED SPÓŁKA AKCYJNA
Device Regulatory Overview
The Infusion set IS PREMIUM with injection site (Model/Catalog Number: 001 921P) 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 921P
- Product Code / EMDN
- A03040199
- Device Name
- Infusion Set
- Database Sync Date
- 2026-08-09 17:08:10
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 Infusion set IS PREMIUM with injection site?
The registered manufacturer of record for Infusion set IS PREMIUM with injection site is MARGOMED SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for Infusion set IS PREMIUM with injection site?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904553993558.
What classification code is assigned to this device?
This device is registered under product classification code A03040199.
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Other Devices by MARGOMED SPÓŁKA AKCYJNA
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