gudid
Primary ID: 491311
BD PrepStain Consumables Kit (UDI 491311)
Manufactured by TRIPATH IMAGING, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BD PrepStain Consumables Kit - Primary ID 491311
Device Regulatory Overview
The BD PrepStain Consumables Kit (Model/Catalog Number: 491311) is a medical device manufactured by TRIPATH IMAGING, INC.. This product is indexed under FDA Product Code / Category Classification MKQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 491311
- Product Code / EMDN
- MKQ
- Device Name
- BD PrepStain Consumables Kit: BD SurePath PreCoat Slides (5 X 96), BD PrepStain Transfer Tips (5 X 96), & BD Settling Chambers (2 X 240)
- 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 PrepStain Consumables Kit?
The registered manufacturer of record for BD PrepStain Consumables Kit is TRIPATH IMAGING, INC..
What is the Primary UDI-DI identifier for BD PrepStain Consumables Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 491311.
What classification code is assigned to this device?
This device is registered under product classification code MKQ.
Similar Classification Devices (MKQ)
Other Devices by TRIPATH IMAGING, INC.
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