GUDIDData
gudid Primary ID: 81343

BF (UDI 81343)

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 81343

Device Regulatory Overview

The BF (Model/Catalog Number: 81343) is a medical device manufactured by Allied Medical, LLC. This product is indexed under FDA Product Code / Category Classification BYX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
81343
Product Code / EMDN
BYX
Device Name
6"CORR TUBING 50/CS
Database Sync Date
2026-08-09 09:00:32

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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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 81343.

What classification code is assigned to this device?

This device is registered under product classification code BYX.

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