gudid
Primary ID: 64375
B&F (UDI 64375)
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 64375
Device Regulatory Overview
The B&F (Model/Catalog Number: 64375) is a medical device manufactured by Allied Medical, LLC. This product is indexed under FDA Product Code / Category Classification BTT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 64375
- Product Code / EMDN
- BTT
- Device Name
- Humidifier
- 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 64375.
What classification code is assigned to this device?
This device is registered under product classification code BTT.
Similar Classification Devices (BTT)
Other Devices by Allied Medical, LLC
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