gudid
Primary ID: MDF621BO
MDF (UDI MDF621BO)
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 MDF621BO
Device Regulatory Overview
The MDF (Model/Catalog Number: MDF621BO) is a medical device manufactured by MDF Instruments Medifriend Inc.. This product is indexed under FDA Product Code / Category Classification KYT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MDF621BO
- Product Code / EMDN
- KYT
- Device Name
- LUMiNiX Professional Diagnostic Penlight, MDFBO
- Database Sync Date
- 2026-08-09 09:04:55
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 MDF621BO.
What classification code is assigned to this device?
This device is registered under product classification code KYT.
Similar Classification Devices (KYT)
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