eudamed_udi
Primary ID: 06430033852200
iCare HOME2 (UDI 06430033852200)
Manufactured by Icare Finland Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for iCare HOME2 - Primary ID 06430033852200
Device Regulatory Overview
The iCare HOME2 (Model/Catalog Number: 260A2) is a medical device manufactured by Icare Finland Oy. This product is indexed under FDA Product Code / Category Classification Z12120122 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 260A2
- Product Code / EMDN
- Z12120122
- Device Name
- iCare HOME2
- Database Sync Date
- 2026-08-09 16:47:26
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 iCare HOME2?
The registered manufacturer of record for iCare HOME2 is Icare Finland Oy.
What is the Primary UDI-DI identifier for iCare HOME2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430033852200.
What classification code is assigned to this device?
This device is registered under product classification code Z12120122.
Similar Classification Devices (Z12120122)
Other Devices by Icare Finland Oy
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