eudamed_udi
Primary ID: 08032804643727
Actizyme (UDI 08032804643727)
Manufactured by Mondial Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Actizyme - Primary ID 08032804643727
Device Regulatory Overview
The Actizyme (Model/Catalog Number: FM0343) is a medical device manufactured by Mondial Srl. This product is indexed under FDA Product Code / Category Classification D0801 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FM0343
- Product Code / EMDN
- D0801
- Device Name
- DISPOSITIVI MEDICI DETERGENTI
- Database Sync Date
- 2026-08-09 16:29:25
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 Actizyme?
The registered manufacturer of record for Actizyme is Mondial Srl.
What is the Primary UDI-DI identifier for Actizyme?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08032804643727.
What classification code is assigned to this device?
This device is registered under product classification code D0801.
Similar Classification Devices (D0801)
Other Devices by Mondial Srl
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