gudid
Primary ID: 491324
BD SurePath Collection Vial Kit 25 (UDI 491324)
Manufactured by TRIPATH IMAGING, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BD SurePath Collection Vial Kit 25 - Primary ID 491324
Device Regulatory Overview
The BD SurePath Collection Vial Kit 25 (Model/Catalog Number: 491324) 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
- 491324
- Product Code / EMDN
- MKQ
- Device Name
- BD SurePath Collection Vial Kit 25
- Database Sync Date
- 2026-08-09 09:59:28
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 SurePath Collection Vial Kit 25?
The registered manufacturer of record for BD SurePath Collection Vial Kit 25 is TRIPATH IMAGING, INC..
What is the Primary UDI-DI identifier for BD SurePath Collection Vial Kit 25?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 491324.
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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