eudamed_udi
Primary ID: 05701780856119
Alterna (UDI 05701780856119)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alterna - Primary ID 05701780856119
Device Regulatory Overview
The Alterna (Model/Catalog Number: 14243) 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
- 14243
- Product Code / EMDN
- A1002010402
- Device Name
- Assura/Alterna (Original) ostomy baseplate convex
- Database Sync Date
- 2026-08-09 16:30:30
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 Alterna?
The registered manufacturer of record for Alterna is Coloplast A/S.
What is the Primary UDI-DI identifier for Alterna?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05701780856119.
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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