eudamed_udi
Primary ID: 05708932752817
Coloplast (UDI 05708932752817)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Coloplast - Primary ID 05708932752817
Device Regulatory Overview
The Coloplast (Model/Catalog Number: AK4100) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification A070199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AK4100
- Product Code / EMDN
- A070199
- Device Name
- TPE connectors
- Database Sync Date
- 2026-08-09 16:46:58
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 Coloplast?
The registered manufacturer of record for Coloplast is Coloplast A/S.
What is the Primary UDI-DI identifier for Coloplast?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05708932752817.
What classification code is assigned to this device?
This device is registered under product classification code A070199.
Similar Classification Devices (A070199)
Other Devices by Coloplast A/S
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