gudid
Primary ID: 505331
Freedom Clear (UDI 505331)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Freedom Clear - Primary ID 505331
Device Regulatory Overview
The Freedom Clear (Model/Catalog Number: 505331) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification NNX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 505331
- Product Code / EMDN
- NNX
- 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 Freedom Clear?
The registered manufacturer of record for Freedom Clear is Coloplast A/S.
What is the Primary UDI-DI identifier for Freedom Clear?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 505331.
What classification code is assigned to this device?
This device is registered under product classification code NNX.
Similar Classification Devices (NNX)
Other Devices by Coloplast A/S
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