gudid
Primary ID: 95050
Coloplast (UDI 95050)
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 95050
Device Regulatory Overview
The Coloplast (Model/Catalog Number: 95050) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification JOK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 95050
- Product Code / EMDN
- JOK
- Device Name
- Database Sync Date
- 2026-08-09 09:12:46
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 95050.
What classification code is assigned to this device?
This device is registered under product classification code JOK.
Similar Classification Devices (JOK)
Other Devices by Coloplast A/S
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