gudid
Primary ID: TF23230
Transfix Continence Sheath (UDI TF23230)
Manufactured by C. R. Bard, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Transfix Continence Sheath - Primary ID TF23230
Device Regulatory Overview
The Transfix Continence Sheath (Model/Catalog Number: TF23230) is a medical device manufactured by C. R. Bard, Inc.. This product is indexed under FDA Product Code / Category Classification NNX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TF23230
- Product Code / EMDN
- NNX
- Device Name
- Transfix All Silicone Self-Adhesive Continence Sheath
- Database Sync Date
- 2026-08-09 09:52:56
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 Transfix Continence Sheath?
The registered manufacturer of record for Transfix Continence Sheath is C. R. Bard, Inc..
What is the Primary UDI-DI identifier for Transfix Continence Sheath?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TF23230.
What classification code is assigned to this device?
This device is registered under product classification code NNX.
Similar Classification Devices (NNX)
Other Devices by C. R. Bard, Inc.
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