MediVisionTech NG Tube Videoassisted System Pack (UDI 04719961230161)
Manufactured by MediVisionTech Co., Ltd.
Device Regulatory Overview
The MediVisionTech NG Tube Videoassisted System Pack (Model/Catalog Number: PAA00102) is a medical device manufactured by MediVisionTech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification G02020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PAA00102
- Product Code / EMDN
- G02020199
- Device Name
- MediVisionTech NG Tube Videoassisted System Pack
- Database Sync Date
- 2026-08-09 16:30:03
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 MediVisionTech NG Tube Videoassisted System Pack?
The registered manufacturer of record for MediVisionTech NG Tube Videoassisted System Pack is MediVisionTech Co., Ltd..
What is the Primary UDI-DI identifier for MediVisionTech NG Tube Videoassisted System Pack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719961230161.
What classification code is assigned to this device?
This device is registered under product classification code G02020199.
Similar Classification Devices (G02020199)
Other Devices by MediVisionTech Co., Ltd.
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