eudamed_udi
Primary ID: 05905386929608
LuxInject syringe (UDI 05905386929608)
Manufactured by MARGOMED SPÓŁKA AKCYJNA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LuxInject syringe - Primary ID 05905386929608
Device Regulatory Overview
The LuxInject syringe (Model/Catalog Number: 010 101) is a medical device manufactured by MARGOMED SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification A020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 010 101
- Product Code / EMDN
- A020199
- Device Name
- Syringe
- Database Sync Date
- 2026-08-09 17:25:38
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 LuxInject syringe?
The registered manufacturer of record for LuxInject syringe is MARGOMED SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for LuxInject syringe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05905386929608.
What classification code is assigned to this device?
This device is registered under product classification code A020199.
Similar Classification Devices (A020199)
Other Devices by MARGOMED SPÓŁKA AKCYJNA
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