eudamed_udi
Primary ID: 05905386929929
Infusion set IS PRO SAFETY (UDI 05905386929929)
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 SAFETY - Primary ID 05905386929929
Device Regulatory Overview
The Infusion set IS PRO SAFETY (Model/Catalog Number: 001 472) 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
- 001 472
- Product Code / EMDN
- A03040199
- Device Name
- Infusion Set
- Database Sync Date
- 2026-08-09 16:58:51
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Infusion set IS PRO SAFETY?
The registered manufacturer of record for Infusion set IS PRO SAFETY is MARGOMED SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for Infusion set IS PRO SAFETY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05905386929929.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint