GUDIDData
gudid Primary ID: 7016C

Dover (UDI 7016C)

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 7016C

Device Regulatory Overview

The Dover (Model/Catalog Number: 7016C) 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
7016C
Product Code / EMDN
PPG
Device Name
Hydrogel Coated Latex Urine Meter Foley Tray with Coude Tip,16 Fr/Ch (5.3 mm), 5 mL Catheter Pre-connected to 2000 mL Drainage Bag with Luer-Slip Sampling
Database Sync Date
2026-08-09 09:42:40

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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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 7016C.

What classification code is assigned to this device?

This device is registered under product classification code PPG.

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