gudid
Primary ID: 491257
BD PrepMate Automated Accessory (UDI 491257)
Manufactured by BECTON, DICKINSON AND COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BD PrepMate Automated Accessory - Primary ID 491257
Device Regulatory Overview
The BD PrepMate Automated Accessory (Model/Catalog Number: 491257) is a medical device manufactured by BECTON, DICKINSON AND COMPANY. This product is indexed under FDA Product Code / Category Classification MKQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 491257
- Product Code / EMDN
- MKQ
- Device Name
- BD PrepMate Automated Accessory Refurbished (100-240V)
- Database Sync Date
- 2026-08-09 10:02:46
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 BD PrepMate Automated Accessory?
The registered manufacturer of record for BD PrepMate Automated Accessory is BECTON, DICKINSON AND COMPANY.
What is the Primary UDI-DI identifier for BD PrepMate Automated Accessory?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 491257.
What classification code is assigned to this device?
This device is registered under product classification code MKQ.
Similar Classification Devices (MKQ)
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