gudid
Primary ID: 490521
BD PrepStain (UDI 490521)
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 - Primary ID 490521
Device Regulatory Overview
The BD PrepStain (Model/Catalog Number: 490521) 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
- 490521
- Product Code / EMDN
- MKQ
- Device Name
- PrepStain Density Reagent
- 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?
The registered manufacturer of record for BD PrepStain is TRIPATH IMAGING, INC..
What is the Primary UDI-DI identifier for BD PrepStain?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 490521.
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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