Reusable Swivel Flex Tube (UDI 04719875346385)
Manufactured by VADI Medical Technology Co., Ltd.
Device Regulatory Overview
The Reusable Swivel Flex Tube (Model/Catalog Number: G-322011-EN) is a medical device manufactured by VADI Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G-322011-EN
- Product Code / EMDN
- R020202
- Device Name
- Reusable Swivel Flex Tube
- Database Sync Date
- 2026-08-09 16:46:14
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 Reusable Swivel Flex Tube?
The registered manufacturer of record for Reusable Swivel Flex Tube is VADI Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for Reusable Swivel Flex Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719875346385.
What classification code is assigned to this device?
This device is registered under product classification code R020202.
Similar Classification Devices (R020202)
Other Devices by VADI Medical Technology Co., Ltd.
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