Dover (UDI 6155)
Manufactured by Cardinal Health 200, LLC
Device Regulatory Overview
The Dover (Model/Catalog Number: 6155) is a medical device manufactured by Cardinal Health 200, LLC. This product is indexed under FDA Product Code / Category Classification PPG 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
- 6155
- Product Code / EMDN
- PPG
- Device Name
- HYDROGEL COATED LATEX FOLEY TRAY, 16 FR (5.3 MM), 5 CC, 2000 ML DRAINAGE BAG, DRAIN SPOUT
- 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 6155.
What classification code is assigned to this device?
This device is registered under product classification code PPG.
Similar Classification Devices (PPG)
Other Devices by Cardinal Health 200, LLC
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