gudid
Primary ID: 50471 / 808
Self-Cath (UDI 50471 / 808)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Self-Cath - Primary ID 50471 / 808
Device Regulatory Overview
The Self-Cath (Model/Catalog Number: 50471 / 808) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification EZD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 50471 / 808
- Product Code / EMDN
- EZD
- Device Name
- No description.
- 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 Self-Cath?
The registered manufacturer of record for Self-Cath is Coloplast A/S.
What is the Primary UDI-DI identifier for Self-Cath?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50471 / 808.
What classification code is assigned to this device?
This device is registered under product classification code EZD.
Similar Classification Devices (EZD)
Other Devices by Coloplast A/S
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