GUDIDData
gudid Primary ID: 81344

BF (UDI 81344)

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 81344

Device Regulatory Overview

The BF (Model/Catalog Number: 81344) 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
81344
Product Code / EMDN
BYX
Device Name
CORR.TUBING 12"SEGMENTED
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
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

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 81344.

What classification code is assigned to this device?

This device is registered under product classification code BYX.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint