eudamed_udi
Primary ID: 08720892175649
Oxion (UDI 08720892175649)
Manufactured by Euromex microscopen bv
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Oxion - Primary ID 08720892175649
Device Regulatory Overview
The Oxion (Model/Catalog Number: OX.xxxx) is a medical device manufactured by Euromex microscopen bv. This product is indexed under FDA Product Code / Category Classification W0202050303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OX.xxxx
- Product Code / EMDN
- W0202050303
- Device Name
- Oxion
- Database Sync Date
- 2026-08-09 16:46:18
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 Oxion?
The registered manufacturer of record for Oxion is Euromex microscopen bv.
What is the Primary UDI-DI identifier for Oxion?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720892175649.
What classification code is assigned to this device?
This device is registered under product classification code W0202050303.
Similar Classification Devices (W0202050303)
Other Devices by Euromex microscopen bv
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint