eudamed_udi
Primary ID: 03760173851034
ZENIT RA (UDI 03760173851034)
Manufactured by ImmunoDiagnostic Systems France
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZENIT RA - Primary ID 03760173851034
Device Regulatory Overview
The ZENIT RA (Model/Catalog Number: 42675) is a medical device manufactured by ImmunoDiagnostic Systems France. This product is indexed under FDA Product Code / Category Classification W0201020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 42675
- Product Code / EMDN
- W0201020102
- Device Name
- IDS-iSYS Multi-Discipline Automated System
- Database Sync Date
- 2026-08-09 16:28:52
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 ZENIT RA?
The registered manufacturer of record for ZENIT RA is ImmunoDiagnostic Systems France.
What is the Primary UDI-DI identifier for ZENIT RA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760173851034.
What classification code is assigned to this device?
This device is registered under product classification code W0201020102.
Similar Classification Devices (W0201020102)
Other Devices by ImmunoDiagnostic Systems France
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint