eudamed_udi
Primary ID: 05905386929912
Infusion set IS PRO AIR PASS (UDI 05905386929912)
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 PRO AIR PASS - Primary ID 05905386929912
Device Regulatory Overview
The Infusion set IS PRO AIR PASS (Model/Catalog Number: 001 471) 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
- 001 471
- Product Code / EMDN
- A03040199
- Device Name
- Infusion Set
- Database Sync Date
- 2026-08-09 17:28:10
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 PRO AIR PASS?
The registered manufacturer of record for Infusion set IS PRO AIR PASS is MARGOMED SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for Infusion set IS PRO AIR PASS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05905386929912.
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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