eudamed_udi
Primary ID: 04063006007417
C_ITE INSIO 3NX ITE (UDI 04063006007417)
Manufactured by Signia GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C_ITE INSIO 3NX ITE - Primary ID 04063006007417
Device Regulatory Overview
The C_ITE INSIO 3NX ITE (Model/Catalog Number: 10956743) is a medical device manufactured by Signia GmbH. This product is indexed under FDA Product Code / Category Classification Y2145060201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10956743
- Product Code / EMDN
- Y2145060201
- Device Name
- CUSTOM
- Database Sync Date
- 2026-08-09 16:47:19
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 C_ITE INSIO 3NX ITE?
The registered manufacturer of record for C_ITE INSIO 3NX ITE is Signia GmbH.
What is the Primary UDI-DI identifier for C_ITE INSIO 3NX ITE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04063006007417.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060201.
Similar Classification Devices (Y2145060201)
Other Devices by Signia GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint