Endobronchial Blocker Tube (UDI 06925816676352)
Manufactured by Well Lead Medical Co., Ltd.
Device Regulatory Overview
The Endobronchial Blocker Tube (Model/Catalog Number: 65110918) is a medical device manufactured by Well Lead Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R010499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 65110918
- Product Code / EMDN
- R010499
- Device Name
- Endobronchial blocker Tube
- Database Sync Date
- 2026-08-09 16:46:53
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 Endobronchial Blocker Tube?
The registered manufacturer of record for Endobronchial Blocker Tube is Well Lead Medical Co., Ltd..
What is the Primary UDI-DI identifier for Endobronchial Blocker Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06925816676352.
What classification code is assigned to this device?
This device is registered under product classification code R010499.
Similar Classification Devices (R010499)
Other Devices by Well Lead Medical Co., Ltd.
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