gudid
Primary ID: N03A011410
Stomach Tube (UDI N03A011410)
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 Stomach Tube - Primary ID N03A011410
Device Regulatory Overview
The Stomach Tube (Model/Catalog Number: N03A011410) is a medical device manufactured by Well Lead Medical Co.,Ltd. This product is indexed under FDA Product Code / Category Classification KNT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N03A011410
- Product Code / EMDN
- KNT
- Device Name
- Opened Tip 14Fr
- Database Sync Date
- 2026-08-09 09:11:04
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 Stomach Tube?
The registered manufacturer of record for Stomach Tube is Well Lead Medical Co.,Ltd.
What is the Primary UDI-DI identifier for Stomach Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is N03A011410.
What classification code is assigned to this device?
This device is registered under product classification code KNT.
Similar Classification Devices (KNT)
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