eudamed_udi
Primary ID: 06417964080834
Kiilto Pro Easydes 5 l (UDI 06417964080834)
Manufactured by KiiltoClean Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kiilto Pro Easydes 5 l - Primary ID 06417964080834
Device Regulatory Overview
The Kiilto Pro Easydes 5 l (Model/Catalog Number: 8083) is a medical device manufactured by KiiltoClean Oy. This product is indexed under FDA Product Code / Category Classification D0701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8083
- Product Code / EMDN
- D0701
- Device Name
- Kiilto Pro Easydes
- Database Sync Date
- 2026-08-09 16:46:33
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 Kiilto Pro Easydes 5 l?
The registered manufacturer of record for Kiilto Pro Easydes 5 l is KiiltoClean Oy.
What is the Primary UDI-DI identifier for Kiilto Pro Easydes 5 l?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06417964080834.
What classification code is assigned to this device?
This device is registered under product classification code D0701.
Similar Classification Devices (D0701)
Other Devices by KiiltoClean Oy
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