eudamed_udi
Primary ID: 05708932936958
SenSura Mio (UDI 05708932936958)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SenSura Mio - Primary ID 05708932936958
Device Regulatory Overview
The SenSura Mio (Model/Catalog Number: 12253) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification A10020302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12253
- Product Code / EMDN
- A10020302
- Device Name
- SenSura Mio flex ostomy bag 2-piece open
- Database Sync Date
- 2026-08-09 16:46:44
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 Mio?
The registered manufacturer of record for SenSura Mio is Coloplast A/S.
What is the Primary UDI-DI identifier for SenSura Mio?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05708932936958.
What classification code is assigned to this device?
This device is registered under product classification code A10020302.
Similar Classification Devices (A10020302)
Other Devices by Coloplast A/S
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