Unspecified Brand (UDI 06976589110017)
Manufactured by Shenzhen OPPO Health Technology Corp., Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: /) is a medical device manufactured by Shenzhen OPPO Health Technology Corp., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12050392 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- Z12050392
- Device Name
- ECG Analyzer
- Database Sync Date
- 2026-08-09 18:07:38
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 Shenzhen OPPO Health Technology Corp., Ltd..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976589110017.
What classification code is assigned to this device?
This device is registered under product classification code Z12050392.
Similar Classification Devices (Z12050392)
Other Devices by Shenzhen OPPO Health Technology Corp., Ltd.
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