Endotracheal Tube (UDI D-ETT5013XX)
Manufactured by Hangzhou Tappa Medical Technology Co , Ltd.
Device Regulatory Overview
The Endotracheal Tube (Model/Catalog Number: ETT5013) is a medical device manufactured by Hangzhou Tappa Medical Technology Co , Ltd.. This product is indexed under FDA Product Code / Category Classification R01030101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ETT5013
- Product Code / EMDN
- R01030101
- Device Name
- Endotracheal Tube
- Database Sync Date
- 2026-08-09 16:29:20
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 Endotracheal Tube?
The registered manufacturer of record for Endotracheal Tube is Hangzhou Tappa Medical Technology Co , Ltd..
What is the Primary UDI-DI identifier for Endotracheal Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-ETT5013XX.
What classification code is assigned to this device?
This device is registered under product classification code R01030101.
Similar Classification Devices (R01030101)
Other Devices by Hangzhou Tappa Medical Technology Co , Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint