SG522DR-G (UDI 06972820963954)
Manufactured by Shenzhen SINO-K Medical Technology Co., Ltd.
Device Regulatory Overview
The SG522DR-G (Model/Catalog Number: 07-10-00) is a medical device manufactured by Shenzhen SINO-K Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12050385 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 07-10-00
- Product Code / EMDN
- Z12050385
- Device Name
- ECG
- Database Sync Date
- 2026-08-09 16:46:25
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 SG522DR-G?
The registered manufacturer of record for SG522DR-G is Shenzhen SINO-K Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for SG522DR-G?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972820963954.
What classification code is assigned to this device?
This device is registered under product classification code Z12050385.
Similar Classification Devices (Z12050385)
Other Devices by Shenzhen SINO-K Medical Technology Co., Ltd.
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