gudid
Primary ID: 491452
BD SurePath Collection Vial (UDI 491452)
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 SurePath Collection Vial - Primary ID 491452
Device Regulatory Overview
The BD SurePath Collection Vial (Model/Catalog Number: 491452) 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
- 491452
- Product Code / EMDN
- MKQ
- Device Name
- BD SurePath Collection Vial
- Database Sync Date
- 2026-08-09 09:31:12
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?
The registered manufacturer of record for BD SurePath Collection Vial is BECTON, DICKINSON AND COMPANY.
What is the Primary UDI-DI identifier for BD SurePath Collection Vial?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 491452.
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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