gudid
Primary ID: 1002261
HMEF (UDI 1002261)
Manufactured by WESTMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HMEF - Primary ID 1002261
Device Regulatory Overview
The HMEF (Model/Catalog Number: 1002261) 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
- 1002261
- Product Code / EMDN
- BYD
- Device Name
- HMEF Adult In-Line Maxi W/Sampling 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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Get API Token Access ($49/mo)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 1002261.
What classification code is assigned to this device?
This device is registered under product classification code BYD.
Similar Classification Devices (BYD)
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