GUDIDData
eudamed_udi Primary ID: 05032384295814

COLUMBIA AGAR WITH SHEEP BLOOD PLUS/ MACCONKEY AGAR W/O SALT (UDI 05032384295814)

Manufactured by Oxoid Deutschland GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COLUMBIA AGAR WITH SHEEP BLOOD PLUS/ MACCONKEY AGAR W/O SALT - Primary ID 05032384295814

Device Regulatory Overview

The COLUMBIA AGAR WITH SHEEP BLOOD PLUS/ MACCONKEY AGAR W/O SALT (Model/Catalog Number: PB5254E) is a medical device manufactured by Oxoid Deutschland GmbH. This product is indexed under FDA Product Code / Category Classification W0104010407 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PB5254E
Product Code / EMDN
W0104010407
Device Name
COLUMBIA AGAR WITH SHEEP BLOOD PLUS/ MACCONKEY AGAR W/O SALT
Database Sync Date
2026-08-09 16:29:21

Full Regulatory Attributes

🔒 Token Gated
{
    "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 COLUMBIA AGAR WITH SHEEP BLOOD PLUS/ MACCONKEY AGAR W/O SALT?

The registered manufacturer of record for COLUMBIA AGAR WITH SHEEP BLOOD PLUS/ MACCONKEY AGAR W/O SALT is Oxoid Deutschland GmbH.

What is the Primary UDI-DI identifier for COLUMBIA AGAR WITH SHEEP BLOOD PLUS/ MACCONKEY AGAR W/O SALT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384295814.

What classification code is assigned to this device?

This device is registered under product classification code W0104010407.

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