gudid
Primary ID: F01B032605
All Silicone Foley Catheter (UDI F01B032605)
Manufactured by Well Lead Medical Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for All Silicone Foley Catheter - Primary ID F01B032605
Device Regulatory Overview
The All Silicone Foley Catheter (Model/Catalog Number: F01B032605) is a medical device manufactured by Well Lead Medical Co.,Ltd. This product is indexed under FDA Product Code / Category Classification EZL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F01B032605
- Product Code / EMDN
- EZL
- Device Name
- 2-way Female 26Fr5-10ml
- Database Sync Date
- 2026-08-09 09:04:58
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 All Silicone Foley Catheter?
The registered manufacturer of record for All Silicone Foley Catheter is Well Lead Medical Co.,Ltd.
What is the Primary UDI-DI identifier for All Silicone Foley Catheter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is F01B032605.
What classification code is assigned to this device?
This device is registered under product classification code EZL.
Similar Classification Devices (EZL)
Other Devices by Well Lead Medical Co.,Ltd
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