eudamed_udi Primary ID: 05212037702122

CHOCOLATE AGAR – SABOURAUD DEXT. AGAR (UDI 05212037702122)

Manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The CHOCOLATE AGAR – SABOURAUD DEXT. AGAR (Model/Catalog Number: 020139) is a medical device manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare. This product is indexed under FDA Product Code / Category Classification W0104010499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 020139
Product Code / EMDN: W0104010499
Device Name: CHOCOLATE AGAR – SABOURAUD DEXT. AGAR
Database Sync Date: 2026-08-09 19:04:25

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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Frequently Asked Questions

Who is the primary manufacturer of CHOCOLATE AGAR – SABOURAUD DEXT. AGAR?

The registered manufacturer of record for CHOCOLATE AGAR – SABOURAUD DEXT. AGAR is G. PAPANIKOLAOU & CO. LP - Bioprepare.

What is the Primary UDI-DI identifier for CHOCOLATE AGAR – SABOURAUD DEXT. AGAR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05212037702122.

What classification code is assigned to this device?

This device is registered under product classification code W0104010499.

Similar Classification Devices (W0104010499)

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