eudamed_udi
Primary ID: 08058964724625
V-MIX 03 (UDI 08058964724625)
Manufactured by G21 S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for V-MIX 03 - Primary ID 08058964724625
Device Regulatory Overview
The V-MIX 03 (Model/Catalog Number: 800047) is a medical device manufactured by G21 S.R.L.. This product is indexed under FDA Product Code / Category Classification P099002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 800047
- Product Code / EMDN
- P099002
- Device Name
- V-MIX
- Database Sync Date
- 2026-08-09 16:28:54
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 V-MIX 03?
The registered manufacturer of record for V-MIX 03 is G21 S.R.L..
What is the Primary UDI-DI identifier for V-MIX 03?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058964724625.
What classification code is assigned to this device?
This device is registered under product classification code P099002.
Similar Classification Devices (P099002)
Other Devices by G21 S.R.L.
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