eudamed_udi
Primary ID: 05708932872799
SenSura Mio Convex (UDI 05708932872799)
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 Convex - Primary ID 05708932872799
Device Regulatory Overview
The SenSura Mio Convex (Model/Catalog Number: 16632) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification A1001020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 16632
- Product Code / EMDN
- A1001020202
- Device Name
- SenSura Mio Convex ostomy bag 1-piece open
- Database Sync Date
- 2026-08-09 16:44:59
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 Convex?
The registered manufacturer of record for SenSura Mio Convex is Coloplast A/S.
What is the Primary UDI-DI identifier for SenSura Mio Convex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05708932872799.
What classification code is assigned to this device?
This device is registered under product classification code A1001020202.
Similar Classification Devices (A1001020202)
Other Devices by Coloplast A/S
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