eudamed_udi
Primary ID: 08050054301082
Ribo Virus (UDI 08050054301082)
Manufactured by Sacace Biotechnologies S.r.l
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ribo Virus - Primary ID 08050054301082
Device Regulatory Overview
The Ribo Virus (Model/Catalog Number: K-2/C) is a medical device manufactured by Sacace Biotechnologies S.r.l. This product is indexed under FDA Product Code / Category Classification W0105900101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K-2/C
- Product Code / EMDN
- W0105900101
- Device Name
- DNA/RNA-Prep NA
- Database Sync Date
- 2026-08-09 16:58:22
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 Ribo Virus?
The registered manufacturer of record for Ribo Virus is Sacace Biotechnologies S.r.l.
What is the Primary UDI-DI identifier for Ribo Virus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050054301082.
What classification code is assigned to this device?
This device is registered under product classification code W0105900101.
Similar Classification Devices (W0105900101)
Other Devices by Sacace Biotechnologies S.r.l
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint