gudid
Primary ID: F01D01181F
PVC Urethral Catheter (UDI F01D01181F)
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 PVC Urethral Catheter - Primary ID F01D01181F
Device Regulatory Overview
The PVC Urethral Catheter (Model/Catalog Number: F01D01181F) is a medical device manufactured by Well Lead Medical Co.,Ltd. This product is indexed under FDA Product Code / Category Classification EZD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F01D01181F
- Product Code / EMDN
- EZD
- Device Name
- Male(standard), 1-way 18Fr
- 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 PVC Urethral Catheter?
The registered manufacturer of record for PVC Urethral Catheter is Well Lead Medical Co.,Ltd.
What is the Primary UDI-DI identifier for PVC Urethral Catheter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is F01D01181F.
What classification code is assigned to this device?
This device is registered under product classification code EZD.
Similar Classification Devices (EZD)
Other Devices by Well Lead Medical Co.,Ltd
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