eudamed_udi
Primary ID: 04056839056400
C_ITE STERLING20 E1 ITC DIR(N4) (UDI 04056839056400)
Manufactured by Sivantos GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C_ITE STERLING20 E1 ITC DIR(N4) - Primary ID 04056839056400
Device Regulatory Overview
The C_ITE STERLING20 E1 ITC DIR(N4) (Model/Catalog Number: 10948478) is a medical device manufactured by Sivantos GmbH. This product is indexed under FDA Product Code / Category Classification Y2145060202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10948478
- Product Code / EMDN
- Y2145060202
- Device Name
- CUSTOM
- Database Sync Date
- 2026-08-09 16:30:43
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 C_ITE STERLING20 E1 ITC DIR(N4)?
The registered manufacturer of record for C_ITE STERLING20 E1 ITC DIR(N4) is Sivantos GmbH.
What is the Primary UDI-DI identifier for C_ITE STERLING20 E1 ITC DIR(N4)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04056839056400.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060202.
Similar Classification Devices (Y2145060202)
Other Devices by Sivantos GmbH
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