eudamed_udi
Primary ID: 06430033850855
Ventica Analytics (UDI 06430033850855)
Manufactured by Icare Finland Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ventica Analytics - Primary ID 06430033850855
Device Regulatory Overview
The Ventica Analytics (Model/Catalog Number: RSP01) is a medical device manufactured by Icare Finland Oy. This product is indexed under FDA Product Code / Category Classification Z12159092 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RSP01
- Product Code / EMDN
- Z12159092
- Device Name
- Ventica Analytics
- Database Sync Date
- 2026-08-09 16:47:05
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 Ventica Analytics?
The registered manufacturer of record for Ventica Analytics is Icare Finland Oy.
What is the Primary UDI-DI identifier for Ventica Analytics?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430033850855.
What classification code is assigned to this device?
This device is registered under product classification code Z12159092.
Similar Classification Devices (Z12159092)
Other Devices by Icare Finland Oy
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