eudamed_udi Primary ID: 05212037703389

CLED AGAR (UDI 05212037703389)

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 CLED AGAR (Model/Catalog Number: 010034) 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: 010034
Product Code / EMDN: W0104010405
Device Name: CLED AGAR
Database Sync Date: 2026-08-09 16:46:42

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 CLED AGAR?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05212037703389.

What classification code is assigned to this device?

This device is registered under product classification code W0104010405.

Similar Classification Devices (W0104010405)

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