eudamed_udi
Primary ID: 05060419220579
Wycath (UDI 05060419220579)
Manufactured by Flexicare Medical Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wycath - Primary ID 05060419220579
Device Regulatory Overview
The Wycath (Model/Catalog Number: W2TM16) is a medical device manufactured by Flexicare Medical Limited. This product is indexed under FDA Product Code / Category Classification U01010601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- W2TM16
- Product Code / EMDN
- U01010601
- Device Name
- Intermittent and Short Term Use Catheters
- Database Sync Date
- 2026-08-09 16:46:55
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 Wycath?
The registered manufacturer of record for Wycath is Flexicare Medical Limited.
What is the Primary UDI-DI identifier for Wycath?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060419220579.
What classification code is assigned to this device?
This device is registered under product classification code U01010601.
Similar Classification Devices (U01010601)
Other Devices by Flexicare Medical Limited
Programmatic Export
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