eudamed_udi
Primary ID: 08052478983608
PRESTOCHILL (UDI 08052478983608)
Manufactured by MILESTONE S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PRESTOCHILL - Primary ID 08052478983608
Device Regulatory Overview
The PRESTOCHILL (Model/Catalog Number: 100850) is a medical device manufactured by MILESTONE S.P.A.. This product is indexed under FDA Product Code / Category Classification W020702 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100850
- Product Code / EMDN
- W020702
- Device Name
- FLASHFREEZE
- Database Sync Date
- 2026-08-09 18:59:10
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of PRESTOCHILL?
The registered manufacturer of record for PRESTOCHILL is MILESTONE S.P.A..
What is the Primary UDI-DI identifier for PRESTOCHILL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052478983608.
What classification code is assigned to this device?
This device is registered under product classification code W020702.
Similar Classification Devices (W020702)
Other Devices by MILESTONE S.P.A.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint