Welllead Reinforced Tracheal Tube (UDI 06936881168437)
Manufactured by Well Lead Medical Co., Ltd.
Device Regulatory Overview
The Welllead Reinforced Tracheal Tube (Model/Catalog Number: A01E06853F) is a medical device manufactured by Well Lead Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R01030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A01E06853F
- Product Code / EMDN
- R01030102
- Device Name
- Reinforced Tracheal Tube
- Database Sync Date
- 2026-08-09 16:28:55
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 Welllead Reinforced Tracheal Tube?
The registered manufacturer of record for Welllead Reinforced Tracheal Tube is Well Lead Medical Co., Ltd..
What is the Primary UDI-DI identifier for Welllead Reinforced Tracheal Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936881168437.
What classification code is assigned to this device?
This device is registered under product classification code R01030102.
Similar Classification Devices (R01030102)
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