gudid
Primary ID: 3305
Dover (UDI 3305)
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 3305
Device Regulatory Overview
The Dover (Model/Catalog Number: 3305) is a medical device manufactured by Cardinal Health, Inc.. This product is indexed under FDA Product Code / Category Classification FCM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3305
- Product Code / EMDN
- FCM
- Device Name
- Urethral Universal Tray,Prepping Components
- Database Sync Date
- 2026-08-09 09:00:28
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 3305.
What classification code is assigned to this device?
This device is registered under product classification code FCM.
Similar Classification Devices (FCM)
Other Devices by Cardinal Health, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint