eudamed_udi Primary ID: 05212037700098

ΒILE ESCULINE AGAR (UDI 05212037700098)

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 ΒILE ESCULINE AGAR (Model/Catalog Number: 010010) is a medical device manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 010010
Product Code / EMDN: W0104010405
Device Name: ΒILE ESCULINE AGAR
Database Sync Date: 2026-08-09 17:14:40

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 ΒILE ESCULINE AGAR?

The registered manufacturer of record for ΒILE ESCULINE AGAR is G. PAPANIKOLAOU & CO. LP - Bioprepare.

What is the Primary UDI-DI identifier for ΒILE ESCULINE AGAR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05212037700098.

What classification code is assigned to this device?

This device is registered under product classification code W0104010405.

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