SurePath Preservative Fluid Collection Vial (UDI 490527)
Manufactured by BECTON, DICKINSON AND COMPANY
Device Regulatory Overview
The SurePath Preservative Fluid Collection Vial (Model/Catalog Number: 490527) 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
- 490527
- Product Code / EMDN
- MKQ
- Device Name
- SurePath GYN Preservative Vial Kit: 10 mL SurePath Preservative Fluid Collection Vials (500)
- 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 SurePath Preservative Fluid Collection Vial?
The registered manufacturer of record for SurePath Preservative Fluid Collection Vial is BECTON, DICKINSON AND COMPANY.
What is the Primary UDI-DI identifier for SurePath Preservative Fluid Collection Vial?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 490527.
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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