gudid Primary ID: 010-105564

HMEF (UDI 010-105564)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The HMEF (Model/Catalog Number: 010-105564) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification BYD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 010-105564
Product Code / EMDN: BYD
Device Name: HMEF Adult In-Line Maxi HMEF W/out Port 350 - 1500 ML VT Range 49.15 ml Dead Space
Database Sync Date: 2026-08-09 09:04:13

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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Frequently Asked Questions

Who is the primary manufacturer of HMEF?

The registered manufacturer of record for HMEF is WESTMED, INC..

What is the Primary UDI-DI identifier for HMEF?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 010-105564.

What classification code is assigned to this device?

This device is registered under product classification code BYD.

Similar Classification Devices (BYD)

Other Devices by WESTMED, INC.

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