gudid
Primary ID: 61399-SF
B&F (UDI 61399-SF)
Manufactured by Allied Medical, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for B&F - Primary ID 61399-SF
Device Regulatory Overview
The B&F (Model/Catalog Number: 61399-SF) is a medical device manufactured by Allied Medical, LLC. This product is indexed under FDA Product Code / Category Classification CAF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 61399-SF
- Product Code / EMDN
- CAF
- Device Name
- Nebulizer Kit
- Database Sync Date
- 2026-08-09 09:00:32
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 B&F?
The registered manufacturer of record for B&F is Allied Medical, LLC.
What is the Primary UDI-DI identifier for B&F?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 61399-SF.
What classification code is assigned to this device?
This device is registered under product classification code CAF.
Similar Classification Devices (CAF)
Other Devices by Allied Medical, LLC
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