eudamed_udi
Primary ID: 04056839099766
C_ITE VIO E212 CIC (UDI 04056839099766)
Manufactured by Sivantos GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C_ITE VIO E212 CIC - Primary ID 04056839099766
Device Regulatory Overview
The C_ITE VIO E212 CIC (Model/Catalog Number: 10964066) is a medical device manufactured by Sivantos GmbH. This product is indexed under FDA Product Code / Category Classification Y2145060201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10964066
- Product Code / EMDN
- Y2145060201
- Device Name
- CUSTOM
- Database Sync Date
- 2026-08-09 16:28:48
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 VIO E212 CIC?
The registered manufacturer of record for C_ITE VIO E212 CIC is Sivantos GmbH.
What is the Primary UDI-DI identifier for C_ITE VIO E212 CIC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04056839099766.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060201.
Similar Classification Devices (Y2145060201)
Other Devices by Sivantos GmbH
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