eudamed_udi
Primary ID: 05708932404143
SenSura Flex (UDI 05708932404143)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SenSura Flex - Primary ID 05708932404143
Device Regulatory Overview
The SenSura Flex (Model/Catalog Number: 113060) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification A1002010402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 113060
- Product Code / EMDN
- A1002010402
- Device Name
- SenSura Flex Xpro ostomy baseplate convex
- Database Sync Date
- 2026-08-09 16:44:50
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 Flex?
The registered manufacturer of record for SenSura Flex is Coloplast A/S.
What is the Primary UDI-DI identifier for SenSura Flex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05708932404143.
What classification code is assigned to this device?
This device is registered under product classification code A1002010402.
Similar Classification Devices (A1002010402)
Other Devices by Coloplast A/S
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