eudamed_udi Primary ID: 05212037700937

GARDNERELLA AGAR (UDI 05212037700937)

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 GARDNERELLA AGAR (Model/Catalog Number: 010044) 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: 010044
Product Code / EMDN: W0104010405
Device Name: GARDNERELLA AGAR
Database Sync Date: 2026-08-09 17:00:03

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 GARDNERELLA AGAR?

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

What is the Primary UDI-DI identifier for GARDNERELLA AGAR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05212037700937.

What classification code is assigned to this device?

This device is registered under product classification code W0104010405.

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