gudid
Primary ID: P4P16XCSDK
Dover (UDI P4P16XCSDK)
Manufactured by Cardinal Health, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dover - Primary ID P4P16XCSDK
Device Regulatory Overview
The Dover (Model/Catalog Number: P4P16XCSDK) is a medical device manufactured by Cardinal Health, Inc.. This product is indexed under FDA Product Code / Category Classification PPG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P4P16XCSDK
- Product Code / EMDN
- PPG
- Device Name
- 100% Silicone Silver-Hydrogel Coated Urine Meter Foley Tray with Coude Tip,16 Fr/Ch (5.3 mm), 5 mL Catheter Pre-connected to 400 mL Urine Meter with 2000 mL Drainage Bag with Adhesive Catheter Securem
- Database Sync Date
- 2026-08-09 09:42:40
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, Inc..
What is the Primary UDI-DI identifier for Dover?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P4P16XCSDK.
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, Inc.
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