gudid
Primary ID: 221365
BD BBL Hektoen Enteric Agar (UDI 221365)
Manufactured by BECTON, DICKINSON AND COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BD BBL Hektoen Enteric Agar - Primary ID 221365
Device Regulatory Overview
The BD BBL Hektoen Enteric Agar (Model/Catalog Number: 221365) is a medical device manufactured by BECTON, DICKINSON AND COMPANY. This product is indexed under FDA Product Code / Category Classification JSI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 221365
- Product Code / EMDN
- JSI
- Device Name
- BD BBL Hektoen Enteric Agar
- Database Sync Date
- 2026-08-09 09:31:12
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BD BBL Hektoen Enteric Agar?
The registered manufacturer of record for BD BBL Hektoen Enteric Agar is BECTON, DICKINSON AND COMPANY.
What is the Primary UDI-DI identifier for BD BBL Hektoen Enteric Agar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 221365.
What classification code is assigned to this device?
This device is registered under product classification code JSI.
Similar Classification Devices (JSI)
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