GUDIDData
eudamed_udi Primary ID: 04043758019487

Centrifuge 5810R (UDI 04043758019487)

Manufactured by Eppendorf SE

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Centrifuge 5810R - Primary ID 04043758019487

Device Regulatory Overview

The Centrifuge 5810R (Model/Catalog Number: 5811 000.827) is a medical device manufactured by Eppendorf SE. This product is indexed under FDA Product Code / Category Classification W02069003 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
5811 000.827
Product Code / EMDN
W02069003
Device Name
Centrifuge 5804; Centrifuge 5804R; Centrifuge 5810; Centrifuge 5810R
Database Sync Date
2026-08-09 16:29:05

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Centrifuge 5810R?

The registered manufacturer of record for Centrifuge 5810R is Eppendorf SE.

What is the Primary UDI-DI identifier for Centrifuge 5810R?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04043758019487.

What classification code is assigned to this device?

This device is registered under product classification code W02069003.

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