Dover (UDI 8888760516)
Manufactured by Cardinal Health 200, LLC
Device Regulatory Overview
The Dover (Model/Catalog Number: 8888760516) is a medical device manufactured by Cardinal Health 200, LLC. This product is indexed under FDA Product Code / Category Classification EZL 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
- 8888760516
- Product Code / EMDN
- EZL
- Device Name
- 100% SILICONE FOLEY CATHETER, 5 CC, 2-WAY, 16 FR (5.3 MM)
- Database Sync Date
- 2026-08-09 09:00:28
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 Dover?
The registered manufacturer of record for Dover is Cardinal Health 200, LLC.
What is the Primary UDI-DI identifier for Dover?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8888760516.
What classification code is assigned to this device?
This device is registered under product classification code EZL.
Similar Classification Devices (EZL)
Other Devices by Cardinal Health 200, LLC
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