gudid
Primary ID: Male Continence Device
C3 (UDI Male Continence Device)
Manufactured by PERSONAL MEDICAL CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C3 - Primary ID Male Continence Device
Device Regulatory Overview
The C3 (Model/Catalog Number: Male Continence Device) is a medical device manufactured by PERSONAL MEDICAL CORP.. This product is indexed under FDA Product Code / Category Classification FHA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Male Continence Device
- Product Code / EMDN
- FHA
- Device Name
- Database Sync Date
- 2026-08-09 09:41:10
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 C3?
The registered manufacturer of record for C3 is PERSONAL MEDICAL CORP..
What is the Primary UDI-DI identifier for C3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Male Continence Device.
What classification code is assigned to this device?
This device is registered under product classification code FHA.
Similar Classification Devices (FHA)
Other Devices by PERSONAL MEDICAL CORP.
Programmatic Export
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