eudamed_udi
Primary ID: 05905386929080
Infusion extension tubing (UDI 05905386929080)
Manufactured by MARGOMED SPÓŁKA AKCYJNA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Infusion extension tubing - Primary ID 05905386929080
Device Regulatory Overview
The Infusion extension tubing (Model/Catalog Number: 004 752) is a medical device manufactured by MARGOMED SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification A03020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 004 752
- Product Code / EMDN
- A03020199
- Device Name
- Extension tubing
- Database Sync Date
- 2026-08-09 16:45:53
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 extension tubing?
The registered manufacturer of record for Infusion extension tubing is MARGOMED SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for Infusion extension tubing?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05905386929080.
What classification code is assigned to this device?
This device is registered under product classification code A03020199.
Similar Classification Devices (A03020199)
Other Devices by MARGOMED SPÓŁKA AKCYJNA
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