Double Lumen Endobronchial Tube (UDI D-DLT0135TJ)
Manufactured by Hangzhou Tappa Medical Technology Co , Ltd.
Device Regulatory Overview
The Double Lumen Endobronchial Tube (Model/Catalog Number: DLT0135) is a medical device manufactured by Hangzhou Tappa Medical Technology Co , Ltd.. This product is indexed under FDA Product Code / Category Classification R01040202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DLT0135
- Product Code / EMDN
- R01040202
- Device Name
- Double Lumen Endobronchial Tube
- Database Sync Date
- 2026-08-09 17:26:54
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 Double Lumen Endobronchial Tube?
The registered manufacturer of record for Double Lumen Endobronchial Tube is Hangzhou Tappa Medical Technology Co , Ltd..
What is the Primary UDI-DI identifier for Double Lumen Endobronchial Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-DLT0135TJ.
What classification code is assigned to this device?
This device is registered under product classification code R01040202.
Similar Classification Devices (R01040202)
Other Devices by Hangzhou Tappa Medical Technology Co , Ltd.
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