BBL (UDI 10382902218088)
Manufactured by Becton, Dickinson and Company
Device Regulatory Overview
The BBL (Model/Catalog Number: 221808) is a medical device manufactured by Becton, Dickinson and Company. This product is indexed under FDA Product Code / Category Classification W0104010402 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 221808
- Product Code / EMDN
- W0104010402
- Device Name
- BD BBLâ„¢ BCYE Agar
- Database Sync Date
- 2026-08-09 16:29:09
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 BBL?
The registered manufacturer of record for BBL is Becton, Dickinson and Company.
What is the Primary UDI-DI identifier for BBL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10382902218088.
What classification code is assigned to this device?
This device is registered under product classification code W0104010402.
Similar Classification Devices (W0104010402)
Other Devices by Becton, Dickinson and Company
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