Patient monitor (UDI 06903053085083)
Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Device Regulatory Overview
The Patient monitor (Model/Catalog Number: BeneVision V200 OR) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BeneVision V200 OR
- Product Code / EMDN
- Z12030201
- Device Name
- BeneVision VMAX
- Database Sync Date
- 2026-08-09 17:35:41
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 Patient monitor?
The registered manufacturer of record for Patient monitor is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..
What is the Primary UDI-DI identifier for Patient monitor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06903053085083.
What classification code is assigned to this device?
This device is registered under product classification code Z12030201.
Similar Classification Devices (Z12030201)
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