eudamed_udi
Primary ID: 08052478982069
MLD3939 3333-5 (UDI 08052478982069)
Manufactured by MILESTONE S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MLD3939 3333-5 - Primary ID 08052478982069
Device Regulatory Overview
The MLD3939 3333-5 (Model/Catalog Number: 100692) is a medical device manufactured by MILESTONE S.P.A.. This product is indexed under FDA Product Code / Category Classification W02079080 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100692
- Product Code / EMDN
- W02079080
- Device Name
- FLASHFREEZE
- Database Sync Date
- 2026-08-09 16:28:44
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 MLD3939 3333-5?
The registered manufacturer of record for MLD3939 3333-5 is MILESTONE S.P.A..
What is the Primary UDI-DI identifier for MLD3939 3333-5?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052478982069.
What classification code is assigned to this device?
This device is registered under product classification code W02079080.
Similar Classification Devices (W02079080)
Other Devices by MILESTONE S.P.A.
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