GUDIDData
eudamed_udi Primary ID: 05032384185122

BRAIN HEART INFUSION AGAR (UDI 05032384185122)

Manufactured by Oxoid Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BRAIN HEART INFUSION AGAR - Primary ID 05032384185122

Device Regulatory Overview

The BRAIN HEART INFUSION AGAR (Model/Catalog Number: CM1136B) is a medical device manufactured by Oxoid Ltd. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CM1136B
Product Code / EMDN
W0104010101
Device Name
BRAIN HEART INFUSION AGAR
Database Sync Date
2026-08-09 16:45:40

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 BRAIN HEART INFUSION AGAR?

The registered manufacturer of record for BRAIN HEART INFUSION AGAR is Oxoid Ltd.

What is the Primary UDI-DI identifier for BRAIN HEART INFUSION AGAR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384185122.

What classification code is assigned to this device?

This device is registered under product classification code W0104010101.

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