GUDIDData
eudamed_udi Primary ID: 05032384447022

NUTRIENT BROTH + GLASS BEADS (UDI 05032384447022)

Manufactured by Oxoid Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NUTRIENT BROTH + GLASS BEADS - Primary ID 05032384447022

Device Regulatory Overview

The NUTRIENT BROTH + GLASS BEADS (Model/Catalog Number: BO1285C) is a medical device manufactured by Oxoid Ltd. This product is indexed under FDA Product Code / Category Classification W0104010306 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BO1285C
Product Code / EMDN
W0104010306
Device Name
NUTRIENT BROTH + GLASS BEADS
Database Sync Date
2026-08-09 16:50:57

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 NUTRIENT BROTH + GLASS BEADS?

The registered manufacturer of record for NUTRIENT BROTH + GLASS BEADS is Oxoid Ltd.

What is the Primary UDI-DI identifier for NUTRIENT BROTH + GLASS BEADS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384447022.

What classification code is assigned to this device?

This device is registered under product classification code W0104010306.

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