SP1719 (UDI 06972820960786)
Manufactured by Shenzhen SINO-K Medical Technology Co., Ltd.
Device Regulatory Overview
The SP1719 (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 C900301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 07-10-00
- Product Code / EMDN
- C900301
- Device Name
- SPO2 Sensor
- Database Sync Date
- 2026-08-09 18:12:31
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 SP1719?
The registered manufacturer of record for SP1719 is Shenzhen SINO-K Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for SP1719?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972820960786.
What classification code is assigned to this device?
This device is registered under product classification code C900301.
Similar Classification Devices (C900301)
Other Devices by Shenzhen SINO-K Medical Technology Co., Ltd.
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