eudamed_udi
Primary ID: 05701780842808
EasiCath (UDI 05701780842808)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EasiCath - Primary ID 05701780842808
Device Regulatory Overview
The EasiCath (Model/Catalog Number: 5388) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification U01010601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5388
- Product Code / EMDN
- U01010601
- Device Name
- EasiCath urinary intermittent drainage catheter
- Database Sync Date
- 2026-08-09 16:47:59
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 EasiCath?
The registered manufacturer of record for EasiCath is Coloplast A/S.
What is the Primary UDI-DI identifier for EasiCath?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05701780842808.
What classification code is assigned to this device?
This device is registered under product classification code U01010601.
Similar Classification Devices (U01010601)
Other Devices by Coloplast A/S
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