gudid
Primary ID: 491097
BD SurePath (UDI 491097)
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 - Primary ID 491097
Device Regulatory Overview
The BD SurePath (Model/Catalog Number: 491097) 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
- 491097
- Product Code / EMDN
- MKQ
- Device Name
- SurePath GYN Preservative Vial Kit with Brush/Spatula
- 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 SurePath?
The registered manufacturer of record for BD SurePath is BECTON, DICKINSON AND COMPANY.
What is the Primary UDI-DI identifier for BD SurePath?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 491097.
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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