gudid
Primary ID: 64021
BF (UDI 64021)
Manufactured by Allied Medical, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BF - Primary ID 64021
Device Regulatory Overview
The BF (Model/Catalog Number: 64021) is a medical device manufactured by Allied Medical, LLC. This product is indexed under FDA Product Code / Category Classification BYP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 64021
- Product Code / EMDN
- BYP
- Device Name
- MOUTHSEAL CUSHION ONLY
- 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 BF?
The registered manufacturer of record for BF is Allied Medical, LLC.
What is the Primary UDI-DI identifier for BF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 64021.
What classification code is assigned to this device?
This device is registered under product classification code BYP.
Similar Classification Devices (BYP)
Other Devices by Allied Medical, LLC
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