Wellead Urethral Catheter (UDI 06944932764286)
Manufactured by Well Lead Medical Co., Ltd.
Device Regulatory Overview
The Wellead Urethral Catheter (Model/Catalog Number: F01A162410) is a medical device manufactured by Well Lead Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification U01010502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F01A162410
- Product Code / EMDN
- U01010502
- Device Name
- Urethral Catheter
- Database Sync Date
- 2026-08-09 16:30:40
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Wellead Urethral Catheter?
The registered manufacturer of record for Wellead Urethral Catheter is Well Lead Medical Co., Ltd..
What is the Primary UDI-DI identifier for Wellead Urethral Catheter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06944932764286.
What classification code is assigned to this device?
This device is registered under product classification code U01010502.
Similar Classification Devices (U01010502)
Other Devices by Well Lead Medical Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint