All Silicone Foley Catheter (UDI 06925816652189)
Manufactured by Well Lead Medical Co., Ltd.
Device Regulatory Overview
The All Silicone Foley Catheter (Model/Catalog Number: AW7112) is a medical device manufactured by Well Lead Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification U010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AW7112
- Product Code / EMDN
- U010299
- Device Name
- All Silicone Foley Catheter
- Database Sync Date
- 2026-08-09 16:28:50
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 06925816652189.
What classification code is assigned to this device?
This device is registered under product classification code U010299.
Similar Classification Devices (U010299)
Other Devices by Well Lead Medical Co., Ltd.
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