Preset (UDI 50382903644167)
Manufactured by Becton, Dickinson and Company
Device Regulatory Overview
The Preset (Model/Catalog Number: 364416) is a medical device manufactured by Becton, Dickinson and Company. This product is indexed under FDA Product Code / Category Classification W0501010103 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 364416
- Product Code / EMDN
- W0501010103
- Device Name
- BD Preset™ and BD A-Line™ Arterial Blood Collection Syringes
- Database Sync Date
- 2026-08-09 18:45:54
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 Preset?
The registered manufacturer of record for Preset is Becton, Dickinson and Company.
What is the Primary UDI-DI identifier for Preset?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50382903644167.
What classification code is assigned to this device?
This device is registered under product classification code W0501010103.
Similar Classification Devices (W0501010103)
Other Devices by Becton, Dickinson and Company
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