gudid
Primary ID: MDF2100451D16
MDF (UDI MDF2100451D16)
Manufactured by MDF Instruments Medifriend Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MDF - Primary ID MDF2100451D16
Device Regulatory Overview
The MDF (Model/Catalog Number: MDF2100451D16) is a medical device manufactured by MDF Instruments Medifriend Inc.. This product is indexed under FDA Product Code / Category Classification DXQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MDF2100451D16
- Product Code / EMDN
- DXQ
- Device Name
- Blood Pressure Cuff, Adult D-Ring, Single Tube, MDF16
- Database Sync Date
- 2026-08-09 09:04:54
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 MDF?
The registered manufacturer of record for MDF is MDF Instruments Medifriend Inc..
What is the Primary UDI-DI identifier for MDF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MDF2100451D16.
What classification code is assigned to this device?
This device is registered under product classification code DXQ.
Similar Classification Devices (DXQ)
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