gudid
Primary ID: A01C02253F
Well Lead Endotracheal Tube (UDI A01C02253F)
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 Well Lead Endotracheal Tube - Primary ID A01C02253F
Device Regulatory Overview
The Well Lead Endotracheal Tube (Model/Catalog Number: A01C02253F) is a medical device manufactured by Well Lead Medical Co.,Ltd. This product is indexed under FDA Product Code / Category Classification BTR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A01C02253F
- Product Code / EMDN
- BTR
- Device Name
- Endotracheal Tubes without Cuff (Nasal)2.5
- 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 Well Lead Endotracheal Tube?
The registered manufacturer of record for Well Lead Endotracheal Tube is Well Lead Medical Co.,Ltd.
What is the Primary UDI-DI identifier for Well Lead Endotracheal Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A01C02253F.
What classification code is assigned to this device?
This device is registered under product classification code BTR.
Similar Classification Devices (BTR)
Other Devices by Well Lead Medical Co.,Ltd
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