GUDIDData
eudamed_udi Primary ID: 30382902574355

BBL (UDI 30382902574355)

Manufactured by Becton Dickinson GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BBL - Primary ID 30382902574355

Device Regulatory Overview

The BBL (Model/Catalog Number: 257435) is a medical device manufactured by Becton Dickinson GmbH. This product is indexed under FDA Product Code / Category Classification W0104010404 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
257435
Product Code / EMDN
W0104010404
Device Name
BD BBL™ CHROMagar™ MRSA II
Database Sync Date
2026-08-09 17:44:01

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 BBL?

The registered manufacturer of record for BBL is Becton Dickinson GmbH.

What is the Primary UDI-DI identifier for BBL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 30382902574355.

What classification code is assigned to this device?

This device is registered under product classification code W0104010404.

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