gudid
Primary ID: 19051
SenSura (UDI 19051)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SenSura - Primary ID 19051
Device Regulatory Overview
The SenSura (Model/Catalog Number: 19051) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification EXB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 19051
- Product Code / EMDN
- EXB
- Device Name
- Database Sync Date
- 2026-08-09 09:12:46
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 SenSura?
The registered manufacturer of record for SenSura is Coloplast A/S.
What is the Primary UDI-DI identifier for SenSura?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 19051.
What classification code is assigned to this device?
This device is registered under product classification code EXB.
Similar Classification Devices (EXB)
Other Devices by Coloplast A/S
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