Unspecified Brand (UDI 16931918102474)
Manufactured by GRI Medical & Electronic Technology Co., Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 4910-NWRTK01) is a medical device manufactured by GRI Medical & Electronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification V080399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4910-NWRTK01
- Product Code / EMDN
- V080399
- Device Name
- Room Turnover Kit
- Database Sync Date
- 2026-08-09 16:28:44
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is GRI Medical & Electronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16931918102474.
What classification code is assigned to this device?
This device is registered under product classification code V080399.
Similar Classification Devices (V080399)
Other Devices by GRI Medical & Electronic Technology Co., Ltd.
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