eudamed_udi
Primary ID: 05905386929301
ProInject syringe (UDI 05905386929301)
Manufactured by MARGOMED SPÓŁKA AKCYJNA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ProInject syringe - Primary ID 05905386929301
Device Regulatory Overview
The ProInject syringe (Model/Catalog Number: 010 060) 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
- 010 060
- Product Code / EMDN
- A020199
- Device Name
- Syringe
- Database Sync Date
- 2026-08-09 16:51:22
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 ProInject syringe?
The registered manufacturer of record for ProInject syringe is MARGOMED SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for ProInject syringe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05905386929301.
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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