eudamed_udi
Primary ID: 07331964006955
Kiilto Pro MD Des Etanol 75+ 1000 ml (UDI 07331964006955)
Manufactured by KiiltoClean Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kiilto Pro MD Des Etanol 75+ 1000 ml - Primary ID 07331964006955
Device Regulatory Overview
The Kiilto Pro MD Des Etanol 75+ 1000 ml (Model/Catalog Number: 695-12) 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
- 695-12
- Product Code / EMDN
- D0701
- Device Name
- Surface disinfectant 75+
- Database Sync Date
- 2026-08-09 18:09:33
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 MD Des Etanol 75+ 1000 ml?
The registered manufacturer of record for Kiilto Pro MD Des Etanol 75+ 1000 ml is KiiltoClean Oy.
What is the Primary UDI-DI identifier for Kiilto Pro MD Des Etanol 75+ 1000 ml?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07331964006955.
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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