GUDIDData
eudamed_udi Primary ID: 62230041012506

C Reactive Protein (CRP) (Latex) (UDI 62230041012506)

Manufactured by Egyptian Company For Biotechnology-Spectrum Diagnostics

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C Reactive Protein (CRP) (Latex) - Primary ID 62230041012506

Device Regulatory Overview

The C Reactive Protein (CRP) (Latex) (Model/Catalog Number: 514 002) is a medical device manufactured by Egyptian Company For Biotechnology-Spectrum Diagnostics. This product is indexed under FDA Product Code / Category Classification W01021109 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
514 002
Product Code / EMDN
W01021109
Device Name
C Reactive Protein (CRP) (Latex)
Database Sync Date
2026-08-09 16:44:57

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 C Reactive Protein (CRP) (Latex)?

The registered manufacturer of record for C Reactive Protein (CRP) (Latex) is Egyptian Company For Biotechnology-Spectrum Diagnostics.

What is the Primary UDI-DI identifier for C Reactive Protein (CRP) (Latex)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 62230041012506.

What classification code is assigned to this device?

This device is registered under product classification code W01021109.

Programmatic Export

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

JSON API Endpoint