gudid
Primary ID: 000433
Penile Clamp (UDI 000433)
Manufactured by C. R. Bard, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Penile Clamp - Primary ID 000433
Device Regulatory Overview
The Penile Clamp (Model/Catalog Number: 000433) is a medical device manufactured by C. R. Bard, Inc.. This product is indexed under FDA Product Code / Category Classification FHA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 000433
- Product Code / EMDN
- FHA
- Device Name
- Penile Clamp
- Database Sync Date
- 2026-08-09 09:52:58
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 Penile Clamp?
The registered manufacturer of record for Penile Clamp is C. R. Bard, Inc..
What is the Primary UDI-DI identifier for Penile Clamp?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 000433.
What classification code is assigned to this device?
This device is registered under product classification code FHA.
Similar Classification Devices (FHA)
Other Devices by C. R. Bard, Inc.
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