GUDIDData
gudid Primary ID: 806510100

Alsevers Solution (UDI 806510100)

Manufactured by Bio-Rad Medical Diagnostics GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alsevers Solution - Primary ID 806510100

Device Regulatory Overview

The Alsevers Solution (Model/Catalog Number: 806510100) is a medical device manufactured by Bio-Rad Medical Diagnostics GmbH. This product is indexed under FDA Product Code / Category Classification KSZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
806510100
Product Code / EMDN
KSZ
Device Name
Suspension medium and stabilizer for red blood cells for TANGO instruments and other immunohaematology methods
Database Sync Date
2026-08-09 09:48:49

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 Alsevers Solution?

The registered manufacturer of record for Alsevers Solution is Bio-Rad Medical Diagnostics GmbH.

What is the Primary UDI-DI identifier for Alsevers Solution?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 806510100.

What classification code is assigned to this device?

This device is registered under product classification code KSZ.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint