Double-lumen Endobronchial Tubes (UDI 06920687340036)
Manufactured by Tianjin Medis Medical Device Co., Ltd.
Device Regulatory Overview
The Double-lumen Endobronchial Tubes (Model/Catalog Number: DLT-L10-35) is a medical device manufactured by Tianjin Medis Medical Device 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
- DLT-L10-35
- Product Code / EMDN
- R01040202
- Device Name
- Double-lumen Endobronchial Tubes
- Database Sync Date
- 2026-08-09 16:46:01
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 Tubes?
The registered manufacturer of record for Double-lumen Endobronchial Tubes is Tianjin Medis Medical Device Co., Ltd..
What is the Primary UDI-DI identifier for Double-lumen Endobronchial Tubes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06920687340036.
What classification code is assigned to this device?
This device is registered under product classification code R01040202.
Similar Classification Devices (R01040202)
Other Devices by Tianjin Medis Medical Device Co., Ltd.
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